Domain ID
Concept Class ID
Vocabulary ID
help_outline
Concept ID
Concept code
Validity
Concept
Valid start27-Apr-2025
Valid end27-Apr-2025

Term connections

Relationship	Relates to	Concept id	Vocabulary
Active possibly_equivalent_to inactive (SNOMED)	Progressive	40607784	SNOMED
Concept replaces	Progressive	40607784	SNOMED
Has Module	SNOMED CT core	40642539	SNOMED
Has clinical course of (SNOMED)	2-methyl-3-hydroxybutyric aciduria	42538941	SNOMED
	ABri amyloidosis	37204495	SNOMED
	ADan amyloidosis	37204554	SNOMED
	ALECT2 amyloidosis	37164101	SNOMED
	ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis	37312166	SNOMED
	Acquired progressive esotropia due to high myopia	1075456	SNOMED
	Acquired progressive kinking of hair	4296766	SNOMED
	Acquired progressive lymphangioma	4297199	SNOMED
	Adenylosuccinate synthetase-like 1-related distal myopathy	37160978	SNOMED
	Adult Alexander disease	37166075	SNOMED
	Adult onset autosomal recessive muscular dystrophy with normal dystrophin	4347187	SNOMED
	Adult spinal muscular atrophy	4311560	SNOMED
	Adult vitelliform macular dystrophy	4339014	SNOMED
	Adult-onset autosomal recessive cerebellar ataxia	37205772	SNOMED
	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy	37110924	SNOMED
	Adult-onset distal myopathy due to valosin containing protein mutation	36674905	SNOMED
	Adult-onset progressive leukoencephalopathy, early-onset deafness	1245327	SNOMED
	Advanced cirrhosis	4048083	SNOMED
	Akinetic-rigid form of Huntington's disease	4046095	SNOMED
	Alcoholic cirrhosis	196463	SNOMED
	Alexander disease	4218753	SNOMED
	Alexander disease type I	37166049	SNOMED
	Alexander disease type II	1075866	SNOMED
	Allan-Herndon-Dudley syndrome	45773358	SNOMED
	Alpha-B crystallin-related late-onset myopathy	37204851	SNOMED
	Amyotrophic lateral sclerosis type 1	37162949	SNOMED
	Amyotrophic lateral sclerosis type 10	37163164	SNOMED
	Amyotrophic lateral sclerosis type 3	37162961	SNOMED
	Amyotrophic lateral sclerosis type 4	37205063	SNOMED
	Amyotrophic lateral sclerosis type 6	37163098	SNOMED
	Amyotrophic lateral sclerosis type 7	37163102	SNOMED
	Amyotrophic lateral sclerosis type 8	37163103	SNOMED
	Amyotrophic lateral sclerosis type 9	37163104	SNOMED
	Amyotrophic lateral sclerosis, parkinsonism, dementia complex	3654598	SNOMED
	Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula	37166121	SNOMED
	Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea	37166119	SNOMED
	Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome	36715354	SNOMED
	Atelosteogenesis	4184046	SNOMED
	Atelosteogenesis type 1	37110773	SNOMED
	Atelosteogenesis type 2	4111311	SNOMED
	Atelosteogenesis type 3	37117239	SNOMED
	Atelosteogenesis/diastrophic dysplasia	4113603	SNOMED
	Atypical Parkinsonism	36716783	SNOMED
	Atypical juvenile parkinsonism	37110776	SNOMED
	Atypical progressive supranuclear palsy syndrome	608052	SNOMED
	Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation	37160970	SNOMED
	Autosomal dominant Charcot-Marie-Tooth disease type 2O	37204281	SNOMED
	Autosomal dominant Charcot-Marie-Tooth disease type 2Q	36676493	SNOMED
	Autosomal dominant Emery-Dreifuss muscular dystrophy	605270	SNOMED
	Autosomal dominant adult-onset proximal spinal muscular atrophy	37205094	SNOMED
	Autosomal dominant amyotrophic lateral sclerosis type 1	37162788	SNOMED
	Autosomal dominant complex hereditary spastic paraplegia	37166048	SNOMED
	Autosomal dominant congenital benign spinal muscular atrophy	35621811	SNOMED
	Autosomal dominant hereditary spastic paraplegia	42537693	SNOMED
	Autosomal dominant late onset Parkinson disease	37396747	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1A	36714666	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1B	37397522	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1C	36714667	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1D	36714668	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1E	36714669	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1F	36714670	SNOMED
	Autosomal dominant limb girdle muscular dystrophy type 1G	36714671	SNOMED
	Autosomal dominant limb-girdle muscular dystrophy type 1H	36675058	SNOMED
	Autosomal dominant mitochondrial myopathy with exercise intolerance	37163895	SNOMED
	Autosomal dominant muscular dystrophy not predominantly limb girdle	4344046	SNOMED
	Autosomal dominant muscular dystrophy with gene located at 5q31	4347190	SNOMED
	Autosomal dominant muscular dystrophy with limb girdle distribution	4347189	SNOMED
	Autosomal dominant neovascular inflammatory vitreoretinopathy	36674904	SNOMED
	Autosomal dominant osteopetrosis type 1	37167248	SNOMED
	Autosomal dominant osteopetrosis type 2	37110722	SNOMED
	Autosomal dominant progressive external ophthalmoplegia	37311116	SNOMED
	Autosomal dominant progressive external ophthalmoplegia type 1	608104	SNOMED
	Autosomal dominant progressive external ophthalmoplegia type 2	603153	SNOMED
	Autosomal dominant progressive external ophthalmoplegia type 3	608102	SNOMED
	Autosomal dominant progressive external ophthalmoplegia type 4	608103	SNOMED
	Autosomal dominant progressive external ophthalmoplegia type 5	608101	SNOMED
	Autosomal dominant spastic paraplegia type 10	37116286	SNOMED
	Autosomal dominant spastic paraplegia type 12	35622059	SNOMED
	Autosomal dominant spastic paraplegia type 13	37204801	SNOMED
	Autosomal dominant spastic paraplegia type 17	4043240	SNOMED
	Autosomal dominant spastic paraplegia type 19	35622060	SNOMED
	Autosomal dominant spastic paraplegia type 29	37116352	SNOMED
	Autosomal dominant spastic paraplegia type 3	37204171	SNOMED
	Autosomal dominant spastic paraplegia type 31	35621812	SNOMED
	Autosomal dominant spastic paraplegia type 36	37109882	SNOMED
	Autosomal dominant spastic paraplegia type 37	35622054	SNOMED
	Autosomal dominant spastic paraplegia type 38	37204738	SNOMED
	Autosomal dominant spastic paraplegia type 4	37109883	SNOMED
	Autosomal dominant spastic paraplegia type 41	35621813	SNOMED
	Autosomal dominant spastic paraplegia type 42	35621814	SNOMED
	Autosomal dominant spastic paraplegia type 6	37116287	SNOMED
	Autosomal dominant spastic paraplegia type 73	37162333	SNOMED
	Autosomal dominant spastic paraplegia type 8	37205775	SNOMED
	Autosomal dominant spastic paraplegia type 9A	37162330	SNOMED
	Autosomal dominant spastic paraplegia type 9B	37162331	SNOMED
	Autosomal recessive Emery-Dreifuss muscular dystrophy	608097	SNOMED
	Autosomal recessive amyotrophic lateral sclerosis type 1	37162789	SNOMED
	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency	37165112	SNOMED
	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency	36676588	SNOMED
	Autosomal recessive cerebellar ataxia, psychomotor delay syndrome	37203830	SNOMED
	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction	37162105	SNOMED
	Autosomal recessive familial Parkinson disease	608078	SNOMED
	Autosomal recessive hereditary spastic paraplegia	37162299	SNOMED
	Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome	36674915	SNOMED
	Autosomal recessive intermediate Charcot-Marie-Tooth disease type C	36676511	SNOMED
	Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy	37163925	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2A	37395782	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2B	37397523	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2C	37399401	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2D	37395781	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2E	36713857	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2F	37397521	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2G	36715054	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2I	37397524	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2J	37117235	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2K	36715055	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2L	37111586	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2M	37111588	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2N	37111587	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2O	37110717	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2P	37111584	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2Q	37111585	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2R	37116273	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2S	37116271	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2T	37116272	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2U	37204689	SNOMED
	Autosomal recessive limb girdle muscular dystrophy type 2Y	37111246	SNOMED
	Autosomal recessive lower motor neuron disease with childhood onset	36675038	SNOMED
	Autosomal recessive muscular dystrophy not predominantly limb girdle	4344282	SNOMED
	Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein	4344279	SNOMED
	Autosomal recessive muscular dystrophy with gene located at 15q	4344044	SNOMED
	Autosomal recessive muscular dystrophy with limb girdle distribution	4347185	SNOMED
	Autosomal recessive myogenic arthrogryposis multiplex congenita	35622689	SNOMED
	Autosomal recessive progressive external ophthalmoplegia	37311114	SNOMED
	Autosomal recessive spastic paraplegia type 11	37399451	SNOMED
	Autosomal recessive spastic paraplegia type 14	37204435	SNOMED
	Autosomal recessive spastic paraplegia type 15	35622636	SNOMED
	Autosomal recessive spastic paraplegia type 18	37116274	SNOMED
	Autosomal recessive spastic paraplegia type 21	35608089	SNOMED
	Autosomal recessive spastic paraplegia type 23	37111579	SNOMED
	Autosomal recessive spastic paraplegia type 24	37205774	SNOMED
	Autosomal recessive spastic paraplegia type 25	37116275	SNOMED
	Autosomal recessive spastic paraplegia type 26	37111578	SNOMED
	Autosomal recessive spastic paraplegia type 27	36680591	SNOMED
	Autosomal recessive spastic paraplegia type 28	35622061	SNOMED
	Autosomal recessive spastic paraplegia type 32	37111577	SNOMED
	Autosomal recessive spastic paraplegia type 35	35622638	SNOMED
	Autosomal recessive spastic paraplegia type 39	36714027	SNOMED
	Autosomal recessive spastic paraplegia type 43	35608091	SNOMED
	Autosomal recessive spastic paraplegia type 44	37109884	SNOMED
	Autosomal recessive spastic paraplegia type 45	35623410	SNOMED
	Autosomal recessive spastic paraplegia type 46	37117173	SNOMED
	Autosomal recessive spastic paraplegia type 48	35622052	SNOMED
	Autosomal recessive spastic paraplegia type 53	37118979	SNOMED
	Autosomal recessive spastic paraplegia type 54	37109885	SNOMED
	Autosomal recessive spastic paraplegia type 55	37109886	SNOMED
	Autosomal recessive spastic paraplegia type 56	37204846	SNOMED
	Autosomal recessive spastic paraplegia type 57	37109887	SNOMED
	Autosomal recessive spastic paraplegia type 58	36674864	SNOMED
	Autosomal recessive spastic paraplegia type 59	36676522	SNOMED
	Autosomal recessive spastic paraplegia type 5A	35622058	SNOMED
	Autosomal recessive spastic paraplegia type 60	37204225	SNOMED
	Autosomal recessive spastic paraplegia type 61	37111582	SNOMED
	Autosomal recessive spastic paraplegia type 62	35608119	SNOMED
	Autosomal recessive spastic paraplegia type 63	37111581	SNOMED
	Autosomal recessive spastic paraplegia type 64	37111580	SNOMED
	Autosomal recessive spastic paraplegia type 66	37204226	SNOMED
	Autosomal recessive spastic paraplegia type 67	35624167	SNOMED
	Autosomal recessive spastic paraplegia type 69	37204213	SNOMED
	Autosomal recessive spastic paraplegia type 70	36674868	SNOMED
	Autosomal recessive spastic paraplegia type 71	37204214	SNOMED
	Autosomal recessive spastic paraplegia type 74	37162269	SNOMED
	Autosomal recessive spastic paraplegia type 75	37162334	SNOMED
	Autosomal recessive spastic paraplegia type 76	37160960	SNOMED
	Autosomal recessive spastic paraplegia type 77	37162343	SNOMED
	Autosomal recessive spastic paraplegia type 78	37161206	SNOMED
	Autosomal recessive spastic paraplegia type 9B	37162332	SNOMED
	Autosomal spastic paraplegia type 30	35622062	SNOMED
	Autosomal spastic paraplegia type 72	37204215	SNOMED
	Axial osteosclerosis	4109184	SNOMED
	BVES-related limb girdle muscular dystrophy	37161418	SNOMED
	Bacterial portal cirrhosis	4055212	SNOMED
	Becker muscular dystrophy	4308668	SNOMED
	Benign autosomal dominant osteopetrosis	4328066	SNOMED
	Benign congenital muscular dystrophy with finger flexion contractures	4344283	SNOMED
	Benign monomelic amyotrophy	4046082	SNOMED
	Benign monomelic amyotrophy of lower limb	37167029	SNOMED
	Benign monomelic amyotrophy of upper limb	37167030	SNOMED
	Benign scapuloperoneal muscular dystrophy	4347193	SNOMED
	Benign scapuloperoneal muscular dystrophy with cardiomyopathy	4345564	SNOMED
	Best vitelliform macular dystrophy	35622071	SNOMED
	Bethlem myopathy	36713650	SNOMED
	Bilateral Sorsby pseudoinflammatory fundus dystrophy	1245477	SNOMED
	Bilateral degenerative progressive high myopia of eyes	36684785	SNOMED
	Bilateral essential iris atrophy	1246377	SNOMED
	Bilateral hemifacial spasm	37169743	SNOMED
	Bilateral progressive external ophthalmoplegia	609299	SNOMED
	Bilateral progressive peripheral pterygium of eyes	37207977	SNOMED
	Biliary cirrhosis	192675	SNOMED
	Biliary cirrhosis of children	4059289	SNOMED
	Birnbaum's syndrome	4164139	SNOMED
	Boomerang dysplasia	4109057	SNOMED
	Boucher Neuhäuser syndrome	37399488	SNOMED
	Bulbospinal neuronopathy	4047740	SNOMED
	CHST3-related skeletal dysplasia	37110891	SNOMED
	CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome	1076367	SNOMED
	COMMAD syndrome	1075860	SNOMED
	Calpain-3-related limb girdle muscular dystrophy D4	37168386	SNOMED
	Capsular portal cirrhosis	4058681	SNOMED
	Cardiac cirrhosis	4252074	SNOMED
	Cardiac portal cirrhosis	4141628	SNOMED
	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	37164876	SNOMED
	Cerebellar ataxia with oculomotor apraxia type 4	37163549	SNOMED
	Charcot-Marie-Tooth disease type 2B5	36675043	SNOMED
	Charcot-Marie-Tooth disease type 2P	37204278	SNOMED
	Childhood-onset autosomal recessive myopathy with external ophthalmoplegia	37206826	SNOMED
	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia	37205771	SNOMED
	Childhood-onset basal ganglia degeneration syndrome	37160930	SNOMED
	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	37160881	SNOMED
	Childhood-onset nemaline myopathy	37162672	SNOMED
	Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome	37162292	SNOMED
	Childhood-onset spasticity with hyperglycinemia	36676582	SNOMED
	Chitty Hall Baraitser syndrome	37396430	SNOMED
	Cholangiolitic cirrhosis	4049282	SNOMED
	Chondrodysplasia with joint dislocations gPAPP type	37204289	SNOMED
	Chronic progressive coccidioidal pneumonia	4221767	SNOMED
	Chronic progressive epilepsia partialis continua	4219724	SNOMED
	Chronic progressive epilepsia partialis continua of childhood	4047894	SNOMED
	Chronic progressive non-hereditary chorea	4144683	SNOMED
	Cirrhosis - non-alcoholic	194692	SNOMED
	Cirrhosis and chronic liver disease	4059284	SNOMED
	Cirrhosis associated with cystic fibrosis	44805713	SNOMED
	Cirrhosis of liver	4064161	SNOMED
	Cirrhosis of liver caused by amiodarone	37111265	SNOMED
	Cirrhosis of liver caused by methotrexate	37117933	SNOMED
	Cirrhosis of liver caused by methyldopa	37111266	SNOMED
	Cirrhosis of liver due to and following cardiac procedure	3656096	SNOMED
	Cirrhosis of liver due to chronic hepatitis C	43531723	SNOMED
	Cirrhosis of liver due to hepatitis B	45772057	SNOMED
	Cirrhosis of liver with primary sclerosing cholangitis	42539566	SNOMED
	Cirrhosis secondary to cholestasis	4153294	SNOMED
	Cirrhotic cardiomyopathy	37110890	SNOMED
	Clonic hemifacial spasm of left facial muscle	761788	SNOMED
	Clonic hemifacial spasm of right facial muscle	761787	SNOMED
	Clonorchiasis with biliary cirrhosis	4292401	SNOMED
	Complicated hereditary spastic paraplegia	4043239	SNOMED
	Congenital cataract with ataxia and deafness syndrome	36714026	SNOMED
	Congenital hereditary muscular dystrophy	78149	SNOMED
	Congenital muscular dystrophy Paradas type	37110894	SNOMED
	Congenital muscular dystrophy due to LMNA mutation	36674283	SNOMED
	Congenital muscular dystrophy type 1A	37204001	SNOMED
	Congenital muscular dystrophy type 1B	35622763	SNOMED
	Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation	619215	SNOMED
	Congenital muscular dystrophy type 1D large gene mutation	619239	SNOMED
	Congenital muscular dystrophy with arthrogryposis multiplex congenita	4344281	SNOMED
	Congenital muscular dystrophy with cerebellar involvement	37204506	SNOMED
	Congenital muscular dystrophy with hyperlaxity	35622006	SNOMED
	Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome	37395848	SNOMED
	Congenital muscular dystrophy with integrin alpha-7 deficiency	36675030	SNOMED
	Congenital muscular dystrophy with intellectual disability	37204504	SNOMED
	Congenital muscular dystrophy with intellectual disability and severe epilepsy	37204238	SNOMED
	Congenital muscular dystrophy without intellectual disability	37204505	SNOMED
	Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome	37160973	SNOMED
	Congenital muscular hypertrophy-cerebral syndrome	4204523	SNOMED
	Congenital myotonic dystrophy	75804	SNOMED
	Congenital pontocerebellar hypoplasia type 14	1245374	SNOMED
	Corticobasal degeneration	4077904	SNOMED
	Corticobasal syndrome	37164298	SNOMED
	Cranio-cervical dystonia with laryngeal and upper limb involvement	37204509	SNOMED
	Craniometadiaphyseal dysplasia	4133493	SNOMED
	Craniometadiaphyseal dysplasia wormian bone type	37110744	SNOMED
	Cruveilhier-Baumgarten syndrome	4163687	SNOMED
	Cryptogenic cirrhosis	4232955	SNOMED
	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome	37160944	SNOMED
	Decompensated cirrhosis of liver	37396401	SNOMED
	Degenerative progressive high myopia	381281	SNOMED
	Degenerative progressive high myopia of left eye	36684725	SNOMED
	Degenerative progressive high myopia of right eye	36684659	SNOMED
	Dementia paralytica juvenilis	4307791	SNOMED
	Dentin dysplasia with sclerotic bone syndrome	36674946	SNOMED
	Desbuquois syndrome	4113729	SNOMED
	Diaphyseal dysplasia	4142627	SNOMED
	Diffuse nodular cirrhosis	4055210	SNOMED
	Distal anoctaminopathy	37204498	SNOMED
	Distal hereditary motor neuropathy type 1	36674792	SNOMED
	Distal hereditary motor neuropathy type 2	37164422	SNOMED
	Distal hereditary motor neuropathy type 7	36674977	SNOMED
	Distal muscular dystrophy	4243215	SNOMED
	Distal muscular dystrophy with juvenile onset	4101902	SNOMED
	Distal muscular dystrophy, Miyoshi type	4008572	SNOMED
	Distal myopathy 2	45765445	SNOMED
	Distal myopathy Welander type	37111375	SNOMED
	Distal myopathy with anterior tibial onset	37204175	SNOMED
	Distal myopathy with posterior leg and anterior hand involvement	37116684	SNOMED
	Distal nebulin myopathy	37204484	SNOMED
	Distal spinal muscular atrophy	4046079	SNOMED
	Drug-induced cirrhosis of liver	4143008	SNOMED
	Duchenne muscular dystrophy	4296473	SNOMED
	Dysplasia of head of femur Meyer type	37396154	SNOMED
	Dystonia 28	37168488	SNOMED
	EVEN-plus syndrome	37166853	SNOMED
	Early cirrhosis	4159158	SNOMED
	Early onset myopathy with fatal cardiomyopathy	45765411	SNOMED
	Early onset parkinsonism and intellectual disability syndrome	37399497	SNOMED
	Early-onset calcifying leukoencephalopathy, skeletal dysplasia	37163908	SNOMED
	Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome	37160886	SNOMED
	Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome	37160933	SNOMED
	Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome	36675179	SNOMED
	Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome	36675141	SNOMED
	Eichsfeld type congenital muscular dystrophy	4347186	SNOMED
	Eiken syndrome	36715312	SNOMED
	Emery-Dreifuss muscular dystrophy	4009185	SNOMED
	Endosteal hyperostoses	4113735	SNOMED
	Endosteal hyperostoses with cerebellar hypoplasia	4113736	SNOMED
	Epidermolysis bullosa simplex with muscular dystrophy	37109579	SNOMED
	Epiphyseal dysplasia	4111316	SNOMED
	Epiphyseal dysplasia, hearing loss, dysmorphism syndrome	35624222	SNOMED
	Epiphyseal dysplasia, microcephalus, nystagmus syndrome	36716110	SNOMED
	Erb's muscular dystrophy	4302459	SNOMED
	Facioscapulohumeral muscular dystrophy	4163266	SNOMED
	Facioscapulohumeral spinal muscular atrophy	4047737	SNOMED
	Facioscapulohumeral spinal muscular atrophy with sensory loss	4047738	SNOMED
	Familial gigantiform cementoma of jaw	37166977	SNOMED
	Familial infantile bilateral striatal necrosis	37163190	SNOMED
	Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome	37160964	SNOMED
	Fatal post-viral neurodegenerative disorder	36676900	SNOMED
	Fatty portal cirrhosis	4058680	SNOMED
	Finnish upper limb onset distal myopathy	35622311	SNOMED
	Fish-eye disease	4029266	SNOMED
	Florid cirrhosis	4294539	SNOMED
	Friedreich ataxia	441554	SNOMED
	Fryns macrocephaly	37396338	SNOMED
	Fukuyama congenital muscular dystrophy	4008570	SNOMED
	Gemignani syndrome	37204181	SNOMED
	General paresis - neurosyphilis	377788	SNOMED
	Giant porokeratosis	4080945	SNOMED
	Glissonian cirrhosis	4203601	SNOMED
	Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome	37160979	SNOMED
	Goldmann-Favre syndrome	4334254	SNOMED
	Granulomatosis disciformis et progressiva	4184973	SNOMED
	Hemifacial spasm	4029329	SNOMED
	Hemifacial spasm of left facial nerve	36686919	SNOMED
	Hemifacial spasm of right facial nerve	36686918	SNOMED
	Hereditary canine spinal muscular atrophy	42573035	SNOMED Veterinary
	Hereditary cerebral amyloid angiopathy, Dutch type	4208824	SNOMED
	Hereditary cerebral amyloid angiopathy, Icelandic type	4164289	SNOMED
	Hereditary cerebral hemorrhage with amyloidosis	37119072	SNOMED
	Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome	36675042	SNOMED
	Hereditary motor and sensory neuropathy type 5	36674990	SNOMED
	Hereditary motor and sensory neuropathy with acrodystrophy	36674991	SNOMED
	Hereditary myopathy limited to females	4347184	SNOMED
	Hereditary progressive mucinous histiocytosis	36675036	SNOMED
	Hereditary progressive muscular dystrophy	80399	SNOMED
	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation	37204522	SNOMED
	Hereditary sensory and autonomic neuropathy with spastic paraplegia	36717042	SNOMED
	Hereditary spastic paraplegia	192901	SNOMED
	Hip dysplasia Beukes type	36715463	SNOMED
	Huntington disease-like 3	36674942	SNOMED
	Huntington's chorea	374341	SNOMED
	Hutterite type of muscular dystrophy	4344045	SNOMED
	Hydrocalycosis	4323996	SNOMED
	Hyperostosis cranialis interna	37163531	SNOMED
	Hyperphosphatasemia tarda	4245856	SNOMED
	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome	36679002	SNOMED
	Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome	36717190	SNOMED
	Hypoxia-associated cirrhosis	4340946	SNOMED
	IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome	1245413	SNOMED
	ITM2B-related amyloidosis	37162253	SNOMED
	ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement	37163232	SNOMED
	Idiopathic copper associated cirrhosis of liver	37396157	SNOMED
	Indian childhood cirrhosis	4268006	SNOMED
	Infantile ascending hereditary spastic paralysis	45766395	SNOMED
	Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	36674869	SNOMED
	Infantile malignant osteopetrosis	4273764	SNOMED
	Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome	1075269	SNOMED
	Infantile osteopetrosis with neuroaxonal dysplasia syndrome	37119061	SNOMED
	Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome	37166815	SNOMED
	Infectious cirrhosis	4340393	SNOMED
	Intellectual disability, spasticity, ectrodactyly syndrome	35622325	SNOMED
	Intermediate X-linked muscular dystrophy	4344277	SNOMED
	Intermediate nemaline myopathy	37162674	SNOMED
	Intrahepatic phlebosclerosis and fibrosis	4342776	SNOMED
	Ji muscular dystrophy	4344605	SNOMED
	Juvenile Alexander disease	37166109	SNOMED
	Juvenile Parkinson's disease	4047751	SNOMED
	Juvenile amyotrophic lateral sclerosis	36713637	SNOMED
	Juvenile amyotrophic lateral sclerosis type 2	37162959	SNOMED
	Juvenile amyotrophic lateral sclerosis type 5	37162963	SNOMED
	Juvenile onset Huntington's disease	4043381	SNOMED
	Juvenile portal cirrhosis	4144116	SNOMED
	KLHL9-related early-onset distal myopathy	35622344	SNOMED
	Keratosis lichenoides chronica	4189461	SNOMED
	Kugelberg-Welander disease	374634	SNOMED
	Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome	37160935	SNOMED
	Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome	37160936	SNOMED
	LIMS2-related limb girdle muscular dystrophy	37161420	SNOMED
	Laennec's cirrhosis, non-alcoholic	4340392	SNOMED
	Laing early-onset distal myopathy	35622700	SNOMED
	Laminin alpha-2 related limb girdle muscular dystrophy R23	37168384	SNOMED
	Langer mesomelic dysplasia syndrome	4242871	SNOMED
	Larsen syndrome	4272804	SNOMED
	Larsen-like osseous dysplasia, short stature syndrome	35622774	SNOMED
	Larsen-like syndrome B3GAT3 type	35622345	SNOMED
	Late onset Huntington's disease	4047752	SNOMED
	Late onset proximal muscular dystrophy with dysarthria	4347191	SNOMED
	Latent cirrhosis	4049419	SNOMED
	Left Sorsby pseudoinflammatory fundus dystrophy	1245476	SNOMED
	Left essential iris atrophy	1246317	SNOMED
	Left progressive external ophthalmoplegia	1077079	SNOMED
	Lenz-Majewski hyperostosis syndrome	4029491	SNOMED
	Lethal Larsen-like syndrome	36714264	SNOMED
	Limb girdle muscular dystrophy due to POMK deficiency	37164804	SNOMED
	Lipoid dermatoarthritis	4224167	SNOMED
	Liver cirrhosis due to classical cystic fibrosis	605193	SNOMED
	Logopenic progressive aphasia	37396532	SNOMED
	Lower motor neuron syndrome with late-adult onset	37204734	SNOMED
	MME-related autosomal dominant Charcot Marie Tooth disease type 2	37160931	SNOMED
	MT-ATP6-related mitochondrial spastic paraplegia	36680600	SNOMED
	Macronodular cirrhosis	4184779	SNOMED
	Manifesting female carrier of X-linked muscular dystrophy	4344278	SNOMED
	Megaconial congenital muscular dystrophy	37164396	SNOMED
	Menopausal muscular dystrophy syndrome	4030587	SNOMED
	Merosin deficient congenital muscular dystrophy	4006462	SNOMED
	Micronodular cirrhosis	4071022	SNOMED
	Microphthalmia with brain atrophy syndrome	36714682	SNOMED
	Mills syndrome	37203943	SNOMED
	Mitchell syndrome	1245376	SNOMED
	Mitochondrial neurogastrointestinal encephalomyopathy syndrome	37397550	SNOMED
	Mixed micro and macronodular cirrhosis	4050640	SNOMED
	Multilobular portal cirrhosis	4148254	SNOMED
	Multiple dislocations with dysplasia	4109180	SNOMED
	Multiple epiphyseal dysplasia	434161	SNOMED
	Multiple epiphyseal dysplasia Al-Gazali type	36714450	SNOMED
	Multiple epiphyseal dysplasia Beighton type	36714451	SNOMED
	Multiple epiphyseal dysplasia Lowry type	35625848	SNOMED
	Multiple epiphyseal dysplasia due to collagen 9 anomaly	35624126	SNOMED
	Multiple epiphyseal dysplasia tarda type IIIa	4196717	SNOMED
	Multiple epiphyseal dysplasia type 1	37396014	SNOMED
	Multiple epiphyseal dysplasia type 4	37396013	SNOMED
	Multiple epiphyseal dysplasia type 5	37396015	SNOMED
	Multiple epiphyseal dysplasia with miniepiphyses	35624150	SNOMED
	Multiple epiphyseal dysplasia with severe proximal femoral dysplasia	35622408	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 4	37163215	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 5	37168389	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 6	37168390	SNOMED
	Multiple progressive hemangiomata	4112769	SNOMED
	Multiple system atrophy, Parkinson's variant	40485457	SNOMED
	Muscle eye brain disease with bilateral multicystic leukodystrophy	37203915	SNOMED
	Muscle-eye-brain disease, congenital muscular dystrophy	4008571	SNOMED
	Muscular dystrophy	4247802	SNOMED
	Muscular dystrophy not predominantly limb girdle in distribution	4345481	SNOMED
	Muscular dystrophy with predominantly proximal limb girdle distribution	4344042	SNOMED
	Muscular dystrophy-deafmutism syndrome	4009657	SNOMED
	Myoclonic epilepsy with ragged red fibers	4044227	SNOMED
	Myopic macular degeneration	4195988	SNOMED
	Myopic macular degeneration of bilateral eyes	36713031	SNOMED
	Myopic macular degeneration of left eye	36687213	SNOMED
	Myopic macular degeneration of right eye	36687212	SNOMED
	Myotonic dystrophy	37161192	SNOMED
	NARP syndrome	4031798	SNOMED
	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy	37163591	SNOMED
	Necrobiotic xanthogranuloma	4300787	SNOMED
	Necrobiotic xanthogranuloma with paraproteinemia	4300788	SNOMED
	Neuronal ceroid lipofuscinosis 8	45771339	SNOMED
	Night blindness, skeletal anomalies, dysmorphism syndrome	37164986	SNOMED
	Non-Alzheimer's progressive dysphasia	4046085	SNOMED
	North American Indian childhood cirrhosis	44783142	SNOMED
	Nutritional cirrhosis	4048057	SNOMED
	O'Sullivan McLeod syndrome	1245326	SNOMED
	Obstructive biliary cirrhosis	4003673	SNOMED
	Occult macular dystrophy	36674817	SNOMED
	Ocular muscular dystrophy	4195688	SNOMED
	Oculopharyngeal muscular dystrophy	4297463	SNOMED
	Oculopharyngeal spinal muscular atrophy	4041684	SNOMED
	Oculopharyngodistal myopathy	35622370	SNOMED
	Odontoleukodystrophy	36716159	SNOMED
	Off-periods in Parkinson disease not responding to oral treatment	37164406	SNOMED
	Orthostatic hypotension co-occurrent and due to Parkinson's disease	36713737	SNOMED
	Osteochondrodysplasia with osteopetrosis	4172752	SNOMED
	Osteomesopycnosis	4113734	SNOMED
	Osteopetrosis	81403	SNOMED
	Osteopetrosis - delayed type	4005119	SNOMED
	Osteopetrosis - intermediate type	4113733	SNOMED
	Osteopetrosis hypogammaglobulinemia syndrome	36674392	SNOMED
	Osteopetrosis with renal tubular acidosis	4111326	SNOMED
	Osteosclerosis	4174195	SNOMED
	Osteosclerotic metaphyseal dysplasia	37165082	SNOMED
	PCNA-related progressive neurodegenerative photosensitivity syndrome	37164095	SNOMED
	PF-ILD-progressive fibrosing interstitial lung disease	37208102	SNOMED
	PLAA-associated neurodevelopmental disorder	37163583	SNOMED
	POGLUT1-related limb girdle muscular dystrophy R21	37160986	SNOMED
	POMGNT2-related limb girdle muscular dystrophy R24	37168385	SNOMED
	PUM1-related cerebellar ataxia	1245414	SNOMED
	PYCR2-related microcephaly, progressive leukoencephalopathy	37165069	SNOMED
	Parana hard skin syndrome	37204372	SNOMED
	Parasitic cirrhosis	4140536	SNOMED
	Parkinson's disease	381270	SNOMED
	Pelvic muscular dystrophy	4102501	SNOMED
	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome	37204229	SNOMED
	Peripheral pterygium, progressive	377291	SNOMED
	Pigment cirrhosis	4300060	SNOMED
	Pigmentary portal cirrhosis	4059285	SNOMED
	Polyglucosan body myopathy type 2	37164075	SNOMED
	Pontine autosomal dominant microangiopathy with leukoencephalopathy	37161067	SNOMED
	Porokeratosis of Mibelli	4213059	SNOMED
	Portal cirrhosis	4304584	SNOMED
	Post poliomyelitis syndrome	4150511	SNOMED
	Posthepatitic cirrhosis	4098583	SNOMED
	Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome	37161068	SNOMED
	Postnecrotic cirrhosis	4313567	SNOMED
	Primary biliary cholangitis	4135822	SNOMED
	Primary hyperplasia of mandibular condyle	37162100	SNOMED
	Primary progressive multiple sclerosis	4178929	SNOMED
	Primary progressive non fluent aphasia	37396465	SNOMED
	Progression of fetal left ventricular outflow tract obstruction	43020511	SNOMED
	Progression of fetal right ventricular outflow tract obstruction	43021871	SNOMED
	Progressive angina	4161973	SNOMED
	Progressive aphasia	4046084	SNOMED
	Progressive aphasia in Alzheimer's disease	4043379	SNOMED
	Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome	37165065	SNOMED
	Progressive avascular necrosis of lunate	37204089	SNOMED
	Progressive bulbar palsy of childhood	4043912	SNOMED
	Progressive cerebellar ataxia with hypogonadism	4047735	SNOMED
	Progressive cerebello-cerebral atrophy	37163193	SNOMED
	Progressive cone dystrophy (without rod involvement)	4143364	SNOMED
	Progressive cone-rod dystrophy	4198347	SNOMED
	Progressive congenital rubella encephalomyelitis	4120303	SNOMED
	Progressive cribriform and zosteriform hyperpigmentation	618890	SNOMED
	Progressive deafness with stapes fixation	37395916	SNOMED
	Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome	40483619	SNOMED
	Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome	36674825	SNOMED
	Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome	37166816	SNOMED
	Progressive external ophthalmoplegia	379027	SNOMED
	Progressive external ophthalmoplegia, myopathy, emaciation syndrome	35608088	SNOMED
	Progressive familial intrahepatic cholestasis type 1	607683	SNOMED
	Progressive familial intrahepatic cholestasis type 2	607718	SNOMED
	Progressive familial intrahepatic cholestasis type 3	37162165	SNOMED
	Progressive familial intrahepatic cholestasis type 4	1245024	SNOMED
	Progressive focal cortical atrophy	42537694	SNOMED
	Progressive internal resorption of tooth caused by bacteria	37167513	SNOMED
	Progressive intrahepatic cholestasis	4253211	SNOMED
	Progressive iris atrophy	439011	SNOMED
	Progressive macular hypomelanosis	37174284	SNOMED
	Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome	37161029	SNOMED
	Progressive multiple sclerosis	37311816	SNOMED
	Progressive muscular atrophy	376679	SNOMED
	Progressive myoclonic epilepsy type 3	37204409	SNOMED
	Progressive myoclonic epilepsy type 5	37204403	SNOMED
	Progressive myoclonic epilepsy type 6	37203831	SNOMED
	Progressive myoclonic epilepsy type 7	37163334	SNOMED
	Progressive myoclonic epilepsy type 8	37204476	SNOMED
	Progressive myoclonic epilepsy type 9	37164081	SNOMED
	Progressive nodular fibrosis of skin	4081232	SNOMED
	Progressive nodular histiocytosis	35622908	SNOMED
	Progressive osteonecrosis of bilateral lunate bones	604655	SNOMED
	Progressive osteonecrosis of left lunate	601177	SNOMED
	Progressive osteonecrosis of right lunate	601176	SNOMED
	Progressive peripheral pterygium of left eye	37207916	SNOMED
	Progressive peripheral pterygium of right eye	37207856	SNOMED
	Progressive pigmentary dermatosis of Schamberg	4271703	SNOMED
	Progressive polyneuropathy with bilateral striatal necrosis	36675041	SNOMED
	Progressive post hemorrhagic ventricular dilatation	4230252	SNOMED
	Progressive relapsing multiple sclerosis	37110514	SNOMED
	Progressive retinal dystrophy due to retinol transport defect	36676632	SNOMED
	Progressive scapulohumeroperoneal distal myopathy	37163545	SNOMED
	Progressive shortening of uterine cervix	44807255	SNOMED
	Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome	37162303	SNOMED
	Progressive supranuclear palsy	40391011	SNOMED
	Progressive supranuclear palsy corticobasal syndrome	608032	SNOMED
	Progressive supranuclear palsy parkinsonism syndrome	608033	SNOMED
	Progressive supranuclear palsy progressive non fluent aphasia	608031	SNOMED
	Progressive systemic sclerosis	40485046	SNOMED
	Proximal myopathy with focal depletion of mitochondria	37162907	SNOMED
	Proximal myotonic myopathy	37395761	SNOMED
	Pseudodiastrophic dysplasia	4113605	SNOMED
	Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome	37162232	SNOMED
	Psychosis co-occurrent and due to Parkinson's disease	36714473	SNOMED
	Pure hereditary spastic paraplegia	4047741	SNOMED
	Pyknodysostosis	4232315	SNOMED
	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations	37204863	SNOMED
	Rett syndrome	4288480	SNOMED
	Reunion Island Larsen-like syndrome	37204694	SNOMED
	Reunion-Indiana Amish type muscular dystrophy	4344606	SNOMED
	Reynolds syndrome	37399445	SNOMED
	Right Sorsby pseudoinflammatory fundus dystrophy	1245475	SNOMED
	Right essential iris atrophy	1246279	SNOMED
	Right progressive external ophthalmoplegia	1077036	SNOMED
	SPOAN and SPOAN-related disorder	37312156	SNOMED
	Scapulohumeral muscular dystrophy	4347192	SNOMED
	Scapulohumeral spinal muscular atrophy	4047739	SNOMED
	Scapuloperoneal muscular dystrophy	4030434	SNOMED
	Scapuloperoneal spinal muscular atrophy	4043913	SNOMED
	Sclerosteosis	4069829	SNOMED
	Secondary biliary cirrhosis	4046123	SNOMED
	Secondary pigmentary retinal degeneration	373193	SNOMED
	Secondary progressive multiple sclerosis	4137855	SNOMED
	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia	37204025	SNOMED
	Semantic dementia	4046091	SNOMED
	Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome	37397207	SNOMED
	Severe autosomal recessive muscular dystrophy of childhood - North African type	4344043	SNOMED
	Severe childhood autosomal recessive muscular dystrophy	4172671	SNOMED
	Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency	37164100	SNOMED
	Severe intellectual disability and progressive spastic paraplegia	36674508	SNOMED
	Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome	36676854	SNOMED
	Severe myopia, generalized joint laxity, short stature syndrome	37163586	SNOMED
	Severe neurodegenerative syndrome with lipodystrophy	36676628	SNOMED
	Severe oculo-renal-cerebellar syndrome	37163149	SNOMED
	Severe scapuloperoneal muscular dystrophy with cardiomyopathy	4345565	SNOMED
	Smoldering systemic mastocytosis	37164748	SNOMED
	Sorsby pseudoinflammatory fundus dystrophy	4108956	SNOMED
	Spastic ataxia, dysarthria due to glutaminase deficiency	37165654	SNOMED
	Spastic paraplegia type 7	37396092	SNOMED
	Spastic paraplegia with Paget disease of bone syndrome	37111591	SNOMED
	Spastic paraplegia with precocious puberty syndrome	37116294	SNOMED
	Spastic paraplegia, facial cutaneous lesion syndrome	35622086	SNOMED
	Spastic paraplegia, glaucoma, intellectual disability syndrome	37116656	SNOMED
	Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome	37166818	SNOMED
	Spastic paraplegia, nephritis, deafness syndrome	37117747	SNOMED
	Spastic paraplegia, neuropathy, poikiloderma syndrome	35622085	SNOMED
	Spastic paraplegia, optic atrophy, neuropathy syndrome	37110771	SNOMED
	Spastic paraplegia, severe developmental delay, epilepsy syndrome	37162298	SNOMED
	Spinal atrophy, ophthalmoplegia, pyramidal syndrome	36675010	SNOMED
	Spinal muscular atrophy	372605	SNOMED
	Spinal muscular atrophy with lower extremity predominance	36675669	SNOMED
	Spinal muscular atrophy with progressive myoclonic epilepsy	45766380	SNOMED
	Spinal muscular atrophy with respiratory distress type 2	36674871	SNOMED
	Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome	37117168	SNOMED
	Spinal muscular atrophy, type II	4027536	SNOMED
	Spinocerebellar ataxia type 41	37163199	SNOMED
	Spinocerebellar ataxia type 42	37163200	SNOMED
	Spinocerebellar ataxia type 43	37163203	SNOMED
	Spinocerebellar ataxia type 45	37168353	SNOMED
	Spinocerebellar ataxia type 46	37168352	SNOMED
	Spondyloepimetaphyseal dysplasia with joint laxity	4111322	SNOMED
	Spondyloepimetaphyseal dysplasia with joint laxity Beighton type	37168828	SNOMED
	Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type	37168829	SNOMED
	Spondyloepimetaphyseal dysplasia with multiple dislocations	35624206	SNOMED
	Spondyloepiphyseal dysplasia Stanescu type	37164084	SNOMED
	Spondyloepiphyseal dysplasia with congenital joint dislocations	45765457	SNOMED
	Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome	36714106	SNOMED
	Sporadic Parkinson disease	37110499	SNOMED
	Steel syndrome	37162796	SNOMED
	Steinert myotonic dystrophy syndrome	79804	SNOMED
	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier	35608124	SNOMED
	Syphilitic cirrhosis	4053079	SNOMED
	Syphilitic portal cirrhosis	4058682	SNOMED
	Tibial muscular dystrophy	44782849	SNOMED
	Toxic cirrhosis	4046016	SNOMED
	Toxic maculopathy of bilateral eyes caused by antimalarial drug	37163329	SNOMED
	Toxic portal cirrhosis	4059287	SNOMED
	Transient infantile osteopetrosis	42709905	SNOMED
	Ullrich congenital muscular dystrophy	4344608	SNOMED
	Unilobular portal cirrhosis	4055209	SNOMED
	Van Bogaert's sclerosing leukoencephalitis	4233538	SNOMED
	Walker-Warburg congenital muscular dystrophy	4009773	SNOMED
	Werdnig-Hoffmann disease	372616	SNOMED
	Western type of congenital muscular dystrophy	4344607	SNOMED
	Wolcott-Rallison dysplasia	4111314	SNOMED
	Worth disease	4109187	SNOMED
	X-linked Emery-Dreifuss muscular dystrophy	608086	SNOMED
	X-linked complex hereditary spastic paraplegia	608090	SNOMED
	X-linked distal arthrogryposis multiplex congenita	36714550	SNOMED
	X-linked distal spinal muscular atrophy type 3	35624164	SNOMED
	X-linked hereditary spastic paraplegia	37110512	SNOMED
	X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome	36714068	SNOMED
	X-linked limb girdle muscular dystrophy with normal dystrophin	4347183	SNOMED
	X-linked muscular dystrophy not predominantly limb girdle	4345563	SNOMED
	X-linked muscular dystrophy with abnormal dystrophin	4344276	SNOMED
	X-linked muscular dystrophy with limb girdle distribution	4344604	SNOMED
	X-linked myopathy with postural muscle atrophy	36674391	SNOMED
	X-linked progressive cerebellar ataxia	37311073	SNOMED
	X-linked pure hereditary spastic paraplegia	608091	SNOMED
	X-linked scapuloperoneal muscular dystrophy	37205074	SNOMED
	X-linked spastic paraplegia type 16	37204800	SNOMED
	X-linked spastic paraplegia type 2	37109776	SNOMED
	X-linked spastic paraplegia type 34	35622055	SNOMED
	Young adult-onset distal hereditary motor neuropathy	36675147	SNOMED
	Young onset Parkinson disease	37395785	SNOMED
Has status	Primitive	40642538	SNOMED
Is a	Behavior descriptors	4116379	SNOMED
	Chronic	4236661	SNOMED
Non-standard to Standard map (OMOP)	Progressive	4114504	SNOMED
Standard to Non-standard map (OMOP)	Progressive	3161593	Nebraska Lexicon
	Progressive	3223647	Nebraska Lexicon
	Progressive	4114504	SNOMED
	Progressive	40607784	SNOMED

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Athena – OHDSI Vocabularies Repository

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