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Concept Class ID
Vocabulary ID
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Concept
Valid start10-Apr-2025
Valid end10-Apr-2025

Term connections

Relationship	Relates to	Concept id	Vocabulary
Associated morphology of (SNOMED)	4H leukodystrophy	37169831	SNOMED
	5-amino-4-imidazole carboxamide ribosiduria	37110832	SNOMED
	AGel amyloidosis	37204494	SNOMED
	AKT2-related familial partial lipodystrophy	37162901	SNOMED
	Achromatopsia	374936	SNOMED
	Acquired generalized lipodystrophy	4336665	SNOMED
	Acquired partial lipodystrophy	4192633	SNOMED
	Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes	4030064	SNOMED
	Adenylosuccinate synthetase-like 1-related distal myopathy	37160978	SNOMED
	Adiposa cornea dystrophy	4048073	SNOMED
	Adolescent X-linked adrenoleukodystrophy	45757735	SNOMED
	Adrenoleukodystrophy	4276356	SNOMED
	Adrenomyeloneuropathy	37168044	SNOMED
	Adult Alexander disease	37166075	SNOMED
	Adult onset autosomal dominant leukodystrophy	40487958	SNOMED
	Adult onset autosomal recessive muscular dystrophy with normal dystrophin	4347187	SNOMED
	Adult vitelliform macular dystrophy	4339014	SNOMED
	Adult-onset distal myopathy due to valosin containing protein mutation	36674905	SNOMED
	Adynamic bone disease	4126449	SNOMED
	Aicardi Goutieres syndrome	4046096	SNOMED
	Aicardi Goutieres syndrome type 1	37162233	SNOMED
	Aicardi Goutieres syndrome type 2	37162234	SNOMED
	Aicardi Goutieres syndrome type 3	37162235	SNOMED
	Aicardi Goutieres syndrome type 4	37162236	SNOMED
	Aicardi Goutieres syndrome type 5	37162237	SNOMED
	Aland Islands eye disease	37110788	SNOMED
	Alexander disease	4218753	SNOMED
	Alexander disease type I	37166049	SNOMED
	Alexander disease type II	1075866	SNOMED
	Algodystrophy of foot	4069529	SNOMED
	Algodystrophy of hand	4068223	SNOMED
	Algodystrophy of knee	4067850	SNOMED
	Alkaline ceramidase 3 deficiency	37165084	SNOMED
	Alstrom syndrome	4270189	SNOMED
	Aluminum-related fracturing osteodystrophy	4128235	SNOMED
	Amaurosis hypertrichosis syndrome	36715352	SNOMED
	Amelogenesis imperfecta co-occurrent with cone rod dystrophy	45771029	SNOMED
	Anterior crocodile shagreen of cornea	4169457	SNOMED
	Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome	36676639	SNOMED
	Arylsulfatase A deficiency	4029879	SNOMED
	Ataxia co-occurrent and due to phytanic acid storage disease	37110506	SNOMED
	Autosomal dominant Emery-Dreifuss muscular dystrophy	605270	SNOMED
	Autosomal dominant deafness with onychodystrophy syndrome	37163211	SNOMED
	Autosomal dominant late-onset retinal degeneration	36714278	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 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 retinitis pigmentosa	4334250	SNOMED
	Autosomal dominant vitreoretinochoroidopathy	46272745	SNOMED
	Autosomal recessive Emery-Dreifuss muscular dystrophy	608097	SNOMED
	Autosomal recessive bestrophinopathy	37117174	SNOMED
	Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome	36675148	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 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 posterior column ataxia and retinitis pigmentosa	37110039	SNOMED
	Autosomal recessive retinitis pigmentosa	4339015	SNOMED
	Autosomal semi-dominant severe lipodystrophic laminopathy	37162902	SNOMED
	BVES-related limb girdle muscular dystrophy	37161418	SNOMED
	Beau's lines	4185564	SNOMED
	Becker muscular dystrophy	4308668	SNOMED
	Bedouin spastic ataxia syndrome	37395871	SNOMED
	Benign concentric annular macular dystrophy	36714337	SNOMED
	Benign congenital muscular dystrophy with finger flexion contractures	4344283	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
	Biallelic RPE65 mutation associated retinal dystrophy	35622786	SNOMED
	Bietti's crystalline retinopathy	4208203	SNOMED
	Bilateral Sorsby pseudoinflammatory fundus dystrophy	1245477	SNOMED
	Bilateral dystrophy of anterior surface of cornea of eyes	37174278	SNOMED
	Bilateral dystrophy of posterior surface of cornea of eyes	37173367	SNOMED
	Bilateral essential iris atrophy	1246377	SNOMED
	Bilateral fundus flavimaculatus of eyes	608791	SNOMED
	Bilateral hereditary dystrophy of cornea of eyes	37174319	SNOMED
	Bilateral iridocorneal endothelial syndrome of eyes	601989	SNOMED
	Bilateral lattice dystrophy of substantia propria of cornea of eyes	37174293	SNOMED
	Bilateral macular dystrophy of substantia propria of cornea of eyes	37172988	SNOMED
	Bilateral stromal dystrophy of substantia propria of cornea of eyes	37172740	SNOMED
	Blue cone monochromatism	37312154	SNOMED
	Bothnia retinal dystrophy	37395995	SNOMED
	Bull's eye macular dystrophy	4334249	SNOMED
	Butterfly-shaped pigmentary macular dystrophy	37111019	SNOMED
	C11ORF73-related autosomal recessive hypomyelinating leukodystrophy	37160940	SNOMED
	CIDEC-related familial partial lipodystrophy	37162903	SNOMED
	Calpain-3-related limb girdle muscular dystrophy D4	37168386	SNOMED
	Canine hypertrophic osteodystrophy	42572821	SNOMED Veterinary
	Cavitating leukodystrophy	42572862	SNOMED Veterinary
	Central cloudy dystrophy of Francois	4168820	SNOMED
	Cerebroretinal vasculopathy	36715304	SNOMED
	Cervical sympathetic dystrophy	4133022	SNOMED
	Chandler syndrome	443429	SNOMED
	Childhood cerebral X-linked adrenoleukodystrophy	45757737	SNOMED
	Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome	37162292	SNOMED
	Cholestanol storage disease	4268608	SNOMED
	Chromosome Xp11.3 microdeletion syndrome	36714526	SNOMED
	Cleft lip retinopathy syndrome	37115759	SNOMED
	Cogan-Reese syndrome	4228180	SNOMED
	Combined corneal dystrophy	4109578	SNOMED
	Complete achromatopsia	37312155	SNOMED
	Complex regional pain syndrome, Type I, of head and/or trunk	43531589	SNOMED
	Complex regional pain syndrome, type I	4175447	SNOMED
	Cone dystrophy	4195048	SNOMED
	Cone dystrophy with supernormal rod response	36714290	SNOMED
	Cone monochromatism	4082133	SNOMED
	Congenital corneal dystrophy	604614	SNOMED
	Congenital generalized lipodystrophy	4111658	SNOMED
	Congenital hereditary endothelial dystrophy	4219835	SNOMED
	Congenital hereditary endothelial dystrophy and perceptive deafness syndrome	36715218	SNOMED
	Congenital hereditary endothelial dystrophy type 1	432628	SNOMED
	Congenital hereditary endothelial dystrophy type 2	4217078	SNOMED
	Congenital hereditary muscular dystrophy	78149	SNOMED
	Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome	37160939	SNOMED
	Congenital macular corneal dystrophy	4317298	SNOMED
	Congenital muscular dystrophy	4344280	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 osteodystrophy	45773180	SNOMED
	Congenital stationary night blindness	374353	SNOMED
	Congenital stromal corneal dystrophy	45773361	SNOMED
	Corneal cerebellar syndrome	36715219	SNOMED
	Corneal dystrophy	380401	SNOMED
	Corneal endothelial dystrophy	443740	SNOMED
	Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome	36676633	SNOMED
	Crocodile shagreen of cornea	4334753	SNOMED
	Crystalline corneal dystrophy	4218853	SNOMED
	Cutis laxa with osteodystrophy	4251484	SNOMED
	DOORS syndrome	36714522	SNOMED
	Deafness with onychodystrophy syndrome	36674396	SNOMED
	Dermatoleukodystrophy	37116362	SNOMED
	Distal anoctaminopathy	37204498	SNOMED
	Distal muscular dystrophy	4243215	SNOMED
	Distal muscular dystrophy with adult onset	4347194	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 early respiratory muscle involvement	37116685	SNOMED
	Distal myopathy with posterior leg and anterior hand involvement	37116684	SNOMED
	Distal nebulin myopathy	37204484	SNOMED
	Disuse osteodystrophy	4246728	SNOMED
	Dominant drusen	4108957	SNOMED
	Dystonia due to metachromatic leucodystrophy	37166936	SNOMED
	Dystrophia unguium	4336254	SNOMED
	Dystrophia unguium, partial	4047507	SNOMED
	Dystrophia unguium, total	4049418	SNOMED
	Dystrophic cardiomyopathy	4108239	SNOMED
	Dystrophy of anterior cornea	443613	SNOMED
	Dystrophy of multiple endocrine glands	37163463	SNOMED
	Dystrophy of vulva	436480	SNOMED
	Early onset myopathy with fatal cardiomyopathy	45765411	SNOMED
	Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome	36715306	SNOMED
	Ectopia lentis, chorioretinal dystrophy, myopia syndrome	36716433	SNOMED
	Eczematous nail dystrophy	37311914	SNOMED
	Eggshell nail	4063455	SNOMED
	Eggshell nails	4274021	SNOMED
	Eichsfeld type congenital muscular dystrophy	4347186	SNOMED
	Elkonyxis	4300907	SNOMED
	Emery-Dreifuss muscular dystrophy	4009185	SNOMED
	Epidermolysis bullosa simplex with muscular dystrophy	37109579	SNOMED
	Epithelial basement membrane dystrophy	381300	SNOMED
	Epithelial recurrent erosion dystrophy	37396189	SNOMED
	Erb's muscular dystrophy	4302459	SNOMED
	Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome	37204325	SNOMED
	Facioscapulohumeral muscular dystrophy	4163266	SNOMED
	Familial benign flecked retina	36674715	SNOMED
	Familial partial lipodystrophy	4174059	SNOMED
	Familial partial lipodystrophy Dunnigan type	37395855	SNOMED
	Familial partial lipodystrophy Kobberling type	37110714	SNOMED
	Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome	37160964	SNOMED
	Finnish upper limb onset distal myopathy	35622311	SNOMED
	Fleck corneal dystrophy	4216892	SNOMED
	Francois syndrome	4113737	SNOMED
	Fuchs' corneal dystrophy	4109696	SNOMED
	Fukuyama congenital muscular dystrophy	4008570	SNOMED
	Fundus albipunctatus	35622759	SNOMED
	Fundus flavimaculatus	4171180	SNOMED
	Fundus flavimaculatus of left eye	1245474	SNOMED
	Fundus flavimaculatus of right eye	1245473	SNOMED
	Fundus pulverulentus	36674718	SNOMED
	Galactocerebroside beta-galactosidase deficiency - early onset	4029117	SNOMED
	Galactosylceramide beta-galactosidase deficiency	4105341	SNOMED
	Gelatinous droplike corneal dystrophy	4171866	SNOMED
	Generalized congenital lipodystrophy with myopathy	608072	SNOMED
	Genetic lipodystrophy	37110561	SNOMED
	Globoid cell leukodystrophy, late-onset	4165746	SNOMED
	Goldmann-Favre syndrome	4334254	SNOMED
	Granular corneal dystrophy	437281	SNOMED
	Granular corneal dystrophy type I	4302370	SNOMED
	Granular corneal dystrophy type II	4288374	SNOMED
	Grayson Wilbrandt corneal dystrophy	36713387	SNOMED
	HSMN IV	4101333	SNOMED
	Hair dystrophy	4048661	SNOMED
	Hepatic osteodystrophy	4150928	SNOMED
	Hereditary corneal dystrophy	374043	SNOMED
	Hereditary macular dystrophy	4173026	SNOMED
	Hereditary myopathy limited to females	4347184	SNOMED
	Hereditary progressive muscular dystrophy	80399	SNOMED
	Hereditary retinal dystrophies in lipidoses	4102654	SNOMED
	Hereditary retinal dystrophy	377270	SNOMED
	Hereditary retinal dystrophy primarily involving retinal pigment epithelium	44782850	SNOMED
	Hereditary retinal dystrophy primarily involving sensory retina	44782851	SNOMED
	Hutterite type of muscular dystrophy	4344045	SNOMED
	Hyaline dystrophy of Bruch's membrane	380711	SNOMED
	Hyaline retinal dystrophy	4102657	SNOMED
	Hypertrophic pulmonary osteopathy	42600394	SNOMED Veterinary
	Hypogonadotropic hypogonadism retinitis pigmentosa syndrome	37118649	SNOMED
	Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum	37110170	SNOMED
	Hypomyelination of early myelinating structures	1245355	SNOMED
	Hypomyelination with brain stem and spinal cord involvement and leg spasticity	36680577	SNOMED
	Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome	36717190	SNOMED
	Hypotrichosis and deafness syndrome	37204690	SNOMED
	Idiopathic hair dystrophy	4048662	SNOMED
	Incomplete achromatopsia	37163258	SNOMED
	Intermediate X-linked muscular dystrophy	4344277	SNOMED
	Iridocorneal endothelial syndrome	4305300	SNOMED
	Iridocorneal endothelial syndrome of left eye	601991	SNOMED
	Iridocorneal endothelial syndrome of right eye	601990	SNOMED
	Ji muscular dystrophy	4344605	SNOMED
	Juvenile Alexander disease	37166109	SNOMED
	Juvenile retinoschisis	4313156	SNOMED
	KLHL9-related early-onset distal myopathy	35622344	SNOMED
	Kandori fleck retina syndrome	35622946	SNOMED
	Keppen Lubinsky syndrome	37163785	SNOMED
	LIMS2-related limb girdle muscular dystrophy	37161420	SNOMED
	LIPE-related familial partial lipodystrophy	37162904	SNOMED
	Laing early-onset distal myopathy	35622700	SNOMED
	Lamellar nail splitting	4218906	SNOMED
	Laminin alpha-2 related limb girdle muscular dystrophy R23	37168384	SNOMED
	Late onset proximal muscular dystrophy with dysarthria	4347191	SNOMED
	Lattice corneal dystrophy	4263345	SNOMED
	Lattice corneal dystrophy Type I	4168018	SNOMED
	Lattice corneal dystrophy Type II	4171402	SNOMED
	Lattice corneal dystrophy Type III	4168801	SNOMED
	Lattice corneal dystrophy, isolated form	436410	SNOMED
	Leber's amaurosis	4108958	SNOMED
	Left Sorsby pseudoinflammatory fundus dystrophy	1245476	SNOMED
	Left cervical sympathetic dystrophy	36687145	SNOMED
	Left essential iris atrophy	1246317	SNOMED
	Leucodystrophy without a known biochemical basis	4144941	SNOMED
	Leukodystrophy	374912	SNOMED
	Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome	35607977	SNOMED
	Limb girdle muscular dystrophy due to POMK deficiency	37164804	SNOMED
	Limb-girdle muscular dystrophy	4246461	SNOMED
	Lipoatrophic diabetes	4131907	SNOMED
	Lipoatrophic diabetes mellitus without complication	44787902	SNOMED
	Lipoatrophy and lipodystrophy	4033030	SNOMED
	Lipodystrophy	134324	SNOMED
	Lipodystrophy caused by antiretroviral drug	37019071	SNOMED
	Lipodystrophy due to juvenile dermatomyositis	606370	SNOMED
	Lipodystrophy due to peptidic growth factors deficiency	37110101	SNOMED
	Lipodystrophy of face	40485079	SNOMED
	Lipodystrophy, intellectual disability, deafness syndrome	36716108	SNOMED
	Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus	4129379	SNOMED
	Lisch epithelial corneal dystrophy	37110100	SNOMED
	Localized lipodystrophy	37311920	SNOMED
	Longitudinal split nail	4309506	SNOMED
	Lupoid onychodystrophy	42573157	SNOMED Veterinary
	Lupus erythematosus-associated nail dystrophy	4299826	SNOMED
	MORM syndrome	37395980	SNOMED
	MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome	1245354	SNOMED
	Macular and peripheral retinoschisis	4334242	SNOMED
	Macular corneal dystrophy	434935	SNOMED
	Macular corneal dystrophy Type I	4170096	SNOMED
	Macular corneal dystrophy Type II	4303793	SNOMED
	Macular retinoschisis	4338898	SNOMED
	Manifesting female carrier of X-linked muscular dystrophy	4344278	SNOMED
	Martinique crinkled retinal pigment epitheliopathy	37162419	SNOMED
	Median canaliform nail dystrophy	4029325	SNOMED
	Median nail dystrophy	4313450	SNOMED
	Median nail dystrophy of Heller	4081082	SNOMED
	Meesman's corneal dystrophy	440408	SNOMED
	Megaconial congenital muscular dystrophy	37164396	SNOMED
	Membranous lipodystrophy	4081237	SNOMED
	Menopausal muscular dystrophy syndrome	4030587	SNOMED
	Merosin deficient congenital muscular dystrophy	4006462	SNOMED
	Metachromatic leukodystrophy	4262609	SNOMED
	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	4180038	SNOMED
	Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency	604586	SNOMED
	Metachromatic leukodystrophy without arylsulfatase deficiency	4308755	SNOMED
	Metachromatic leukodystrophy, adult type	4085741	SNOMED
	Metachromatic leukodystrophy, congenital type	4238363	SNOMED
	Metachromatic leukodystrophy, juvenile type	4185906	SNOMED
	Metachromatic leukodystrophy, late infantile type	4166222	SNOMED
	Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome	36675066	SNOMED
	Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome	36674513	SNOMED
	Mixed renal osteodystrophy	46270969	SNOMED
	Morquio syndrome	4292105	SNOMED
	Mucopolysaccharidosis, MPS-IV-A	4219277	SNOMED
	Mucopolysaccharidosis, MPS-IV-B	4031815	SNOMED
	Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus	37109645	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 4	37163215	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 5	37168389	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
	Myotonic dystrophy	37161192	SNOMED
	NARP syndrome	4031798	SNOMED
	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy	37163591	SNOMED
	Nail dystrophy associated with bullous dermatoses	4300903	SNOMED
	Nail dystrophy associated with dermatological disease	4297819	SNOMED
	Nail dystrophy caused by chemical	1244865	SNOMED
	Nail dystrophy co-occurrent with reactive arthritis triad	4223486	SNOMED
	Nail dystrophy due to Darier's disease	4300453	SNOMED
	Nail dystrophy due to benign familial pemphigus	4297930	SNOMED
	Nail dystrophy due to cytotoxic therapy	4299698	SNOMED
	Nail dystrophy due to epidermolysis bullosa	37165465	SNOMED
	Nail dystrophy due to graft-versus-host disease	4297507	SNOMED
	Nail dystrophy due to habit tic	4299572	SNOMED
	Nail dystrophy due to lichen nitidus	4221668	SNOMED
	Nail dystrophy due to lichen striatus	4223488	SNOMED
	Nail dystrophy due to nail biting	4221973	SNOMED
	Nail dystrophy due to nail picking	4295322	SNOMED
	Nail dystrophy due to pityriasis rubra pilaris	4297500	SNOMED
	Nail dystrophy due to sarcoidosis	4221669	SNOMED
	Nail dystrophy due to secondary syphilis	4298863	SNOMED
	Nail dystrophy due to trauma	4291283	SNOMED
	Neonatal adrenoleukodystrophy	4029887	SNOMED
	Neuroaxonal leukodystrophy	4043401	SNOMED
	Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy	37163798	SNOMED
	North Carolina macular dystrophy	4208202	SNOMED
	Nutcracker nails	4033855	SNOMED
	O/E - nails - pitting	4063716	SNOMED
	Occult macular dystrophy	36674817	SNOMED
	Ocular muscular dystrophy	4195688	SNOMED
	Oculopharyngeal muscular dystrophy	4297463	SNOMED
	Oculopharyngodistal myopathy	35622370	SNOMED
	Oculotrichodysplasia	36716158	SNOMED
	Odontoleukodystrophy	36716159	SNOMED
	Oguchi's disease	4109112	SNOMED
	Oligocone trichromacy	36716161	SNOMED
	Onychogryposis	4200238	SNOMED
	Ophthalmomandibulomelic dysplasia	37395886	SNOMED
	Ossification anomaly with psychomotor developmental delay syndrome	36716189	SNOMED
	Osteitis fibrosa cystica	4223082	SNOMED
	Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome	36717531	SNOMED
	Osteodystrophy	75924	SNOMED
	Ovarioleukodystrophy	608037	SNOMED
	POGLUT1-related limb girdle muscular dystrophy R21	37160986	SNOMED
	POMGNT2-related limb girdle muscular dystrophy R24	37168385	SNOMED
	PPARG-related familial partial lipodystrophy	37162900	SNOMED
	Panniculitis induced localized lipodystrophy	37204373	SNOMED
	Partial face-sparing lipodystrophy	4318713	SNOMED
	Pattern dystrophy of macula	4335593	SNOMED
	Pelizaeus Merzbacher like disease	37397028	SNOMED
	Pelizaeus Merzbacher like disease due to AIMP1 mutation	3655824	SNOMED
	Pelizaeus Merzbacher like disease due to GJC2 mutation	3655825	SNOMED
	Pelizaeus Merzbacher like disease due to HSPD1 mutation	3655822	SNOMED
	Pelizaeus Merzbacher like disease due to SLC16A2 mutation	3655823	SNOMED
	Pelizaeus-Merzbacher disease	4275445	SNOMED
	Pelizaeus-Merzbacher disease in female carrier	604909	SNOMED
	Pelizaeus-Merzbacher disease null syndrome	604652	SNOMED
	Pelizaeus-Merzbacher disease, classic form	4226864	SNOMED
	Pelizaeus-Merzbacher disease, connatal variant	4242743	SNOMED
	Pelvic muscular dystrophy	4102501	SNOMED
	Perilipin 1 related familial partial lipodystrophy	37204732	SNOMED
	Peripapillary choroidal dystrophy	37164705	SNOMED
	Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease	35623047	SNOMED
	Pigmentary retinal dystrophy	373472	SNOMED
	Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome	37164291	SNOMED
	Pitting of nail due to alopecia areata	37165226	SNOMED
	Pitting of nails	4233101	SNOMED
	Polymorphous corneal dystrophy	4105592	SNOMED
	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome	37109673	SNOMED
	Posterior amorphous corneal dystrophy	36714175	SNOMED
	Posterior corneal dystrophy	45757727	SNOMED
	Posterior crocodile shagreen of cornea	4228766	SNOMED
	Pre-descemet's corneal dystrophy	4338880	SNOMED
	Primary ciliary dyskinesia and retinitis pigmentosa syndrome	36714163	SNOMED
	Primary hair dystrophy	4047505	SNOMED
	Progeroid and marfanoid aspect, lipodystrophy syndrome	36674384	SNOMED
	Progressive bifocal chorioretinal atrophy	36714153	SNOMED
	Progressive cone dystrophy (without rod involvement)	4143364	SNOMED
	Progressive cone-rod dystrophy	4198347	SNOMED
	Progressive iris atrophy	439011	SNOMED
	Progressive retinal dystrophy due to retinol transport defect	36676632	SNOMED
	Progressive rod dystrophy	4336006	SNOMED
	Progressive scapulohumeroperoneal distal myopathy	37163545	SNOMED
	Proximal myotonic myopathy	37395761	SNOMED
	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa	37163799	SNOMED
	Psoriatic nail dystrophy	4031140	SNOMED
	Psoriatic nail pitting	4031650	SNOMED
	RARS-related autosomal recessive hypomyelinating leukodystrophy	37163800	SNOMED
	RAVINE syndrome	37399469	SNOMED
	RHYNS syndrome	37109994	SNOMED
	RNA polymerase III-related leukodystrophy	46273291	SNOMED
	Racket nail	4197958	SNOMED
	Reflex sympathetic dystrophy of lower extremity	443446	SNOMED
	Reis-Bucklers' corneal dystrophy	4338879	SNOMED
	Renal dysplasia and retinal aplasia	4128229	SNOMED
	Renal osteodystrophy	197921	SNOMED
	Renal osteodystrophy due to hyperparathyroidism	37163454	SNOMED
	Renal osteodystrophy with high bone turnover	619681	SNOMED
	Renal osteodystrophy with low bone turnover	619683	SNOMED
	Renal osteodystrophy with normal bone turnover	619682	SNOMED
	Reticular dystrophy of retinal pigment epithelium	37109698	SNOMED
	Retinal dystrophy	380395	SNOMED
	Retinal dystrophy due to GM2 gangliosidosis	37162375	SNOMED
	Retinal dystrophy due to systemic disorder	46274005	SNOMED
	Retinal dystrophy in cerebroretinal lipidosis	439689	SNOMED
	Retinal dystrophy in systemic lipidosis	443895	SNOMED
	Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies	36676857	SNOMED
	Retinal macular dystrophy type 2	36674762	SNOMED
	Retinal pigment epithelial dystrophy	45757713	SNOMED
	Retinitis pigmentosa	4103381	SNOMED
	Retinitis pigmentosa due to systemic disease	37164695	SNOMED
	Retinitis pigmentosa of bilateral eyes	761384	SNOMED
	Retinitis pigmentosa of left eye	761383	SNOMED
	Retinitis pigmentosa of right eye	765078	SNOMED
	Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome	37160945	SNOMED
	Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome	37109996	SNOMED
	Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome	37163797	SNOMED
	Retinitis pigmentosa-deafness syndrome	4240613	SNOMED
	Retinitis pigmentosa-deafness syndrome type 3	605187	SNOMED
	Retinitis pigmentosa-deafness-ataxia syndrome	4218925	SNOMED
	Retinitis punctata albescens	37395938	SNOMED
	Retinohepatoendocrinologic syndrome	37109995	SNOMED
	Reunion-Indiana Amish type muscular dystrophy	4344606	SNOMED
	Right Sorsby pseudoinflammatory fundus dystrophy	1245475	SNOMED
	Right cervical sympathetic dystrophy	36687146	SNOMED
	Right essential iris atrophy	1246279	SNOMED
	Ring-like corneal dystrophy	4192366	SNOMED
	Robinson nail dystrophy-deafness syndrome	4097391	SNOMED
	Rod dystrophy	4196128	SNOMED
	Rod monochromatism	4009866	SNOMED
	Sagliker syndrome	37163330	SNOMED
	Saldino-Mainzer dysplasia	4111320	SNOMED
	Scapulohumeral muscular dystrophy	4347192	SNOMED
	Scapuloperoneal muscular dystrophy	4030434	SNOMED
	Schnyder crystalline cornea dystrophy	4304093	SNOMED
	Scleroderma-associated nail dystrophy	4296515	SNOMED
	Secondary hair dystrophy	4047506	SNOMED
	Sensory retinal dystrophy	45757731	SNOMED
	Severe autosomal recessive muscular dystrophy of childhood - North African type	4344043	SNOMED
	Severe childhood autosomal recessive muscular dystrophy	4172671	SNOMED
	Severe early childhood onset retinal dystrophy	37396748	SNOMED
	Severe neurodegenerative syndrome with lipodystrophy	36676628	SNOMED
	Severe scapuloperoneal muscular dystrophy with cardiomyopathy	4345565	SNOMED
	Shoulder-hand syndrome	4050999	SNOMED
	Sorsby pseudoinflammatory fundus dystrophy	4108956	SNOMED
	Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome	37109775	SNOMED
	Sphingolipid activator protein 1 deficiency	4286511	SNOMED
	Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome	36714106	SNOMED
	Spondylometaphyseal dysplasia, corneal dystrophy syndrome	37167957	SNOMED
	Spongy degeneration of central nervous system	4214740	SNOMED
	Squamous cell hyperplasia of vulva	4174576	SNOMED
	Stargardt's disease	4289290	SNOMED
	Steinert myotonic dystrophy syndrome	79804	SNOMED
	Stern Lubinsky Durrie syndrome	37109746	SNOMED
	Stromal corneal dystrophy	438428	SNOMED
	Subepithelial mucinous corneal dystrophy	37109744	SNOMED
	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier	35608124	SNOMED
	TUBB4A-related leukodystrophy	35625955	SNOMED
	Tapetoretinal dystrophy	4108959	SNOMED
	Thiel-Behnke corneal dystrophy	4213367	SNOMED
	Tibial muscular dystrophy	44782849	SNOMED
	Toxic liver dystrophy of swine	42572601	SNOMED Veterinary
	Triphalangeal thumbs with onychodystrophy	4034567	SNOMED
	Twenty nail dystrophy	4033856	SNOMED
	Type III transitional Pelizaeus-Merzbacher disease	4047883	SNOMED
	Type IV adult Pelizaeus-Merzbacher disease	4044073	SNOMED
	Type V atypical Pelizaeus-Merzbacher disease	4044075	SNOMED
	Type VI Cockayne Pelizaeus-Merzbacher disease	4047884	SNOMED
	Ullrich congenital muscular dystrophy	4344608	SNOMED
	Usher syndrome type 1	4339018	SNOMED
	Usher syndrome type 1F	37172415	SNOMED
	Usher syndrome type 2	4334251	SNOMED
	VPS11-related autosomal recessive hypomyelinating leukodystrophy	37162291	SNOMED
	Vanishing white matter disease	40492344	SNOMED
	Vitelliform dystrophy	4231849	SNOMED
	Vitreoretinal dystrophy	373772	SNOMED
	Walker-Warburg congenital muscular dystrophy	4009773	SNOMED
	Western type of congenital muscular dystrophy	4344607	SNOMED
	X-linked Emery-Dreifuss muscular dystrophy	608086	SNOMED
	X-linked endothelial corneal dystrophy	36717051	SNOMED
	X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency	37115758	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 retinitis pigmentosa	4339016	SNOMED
	X-linked retinitis pigmentosa heterozygote	4339017	SNOMED
	X-linked scapuloperoneal muscular dystrophy	37205074	SNOMED
	X-linked spastic paraplegia type 2	37109776	SNOMED
Has Module	SNOMED CT core	40642539	SNOMED
Has status	Primitive	40642538	SNOMED
Is a	Degenerative abnormality	4030637	SNOMED
Non-standard to Standard map (OMOP)	Dystrophy	4186313	SNOMED
Standard to Non-standard map (OMOP)	Dystrophy	3446205	Nebraska Lexicon
	Dystrophy	4186313	SNOMED
Subsumes	Hyperplastic dystrophy	4066622	SNOMED
	Pseudohypertrophic dystrophy	4076378	SNOMED

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Definitions

Data Analysis System: a computer system that is used to analyze records or other data, but not if that system is also a Data Creation System

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Term connections

Athena – OHDSI Vocabularies Repository

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