keyboard_backspaceDisorder of digestive system specific to fetus OR newborn

Domain IDCondition
Concept Class IDDisorder
Vocabulary ID
SNOMED
help_outline
Systematic Nomenclature of Medicine - Clinical Terms (IHTSDO)
2024-08-01 SNOMED CT International Edition; 2024-09-01 SNOMED CT US Edition; 2024-09-25 SNOMED CT UK Edition
http://www.nlm.nih.gov/research/umls/licensedcontent/umlsknowledgesources.html
Concept ID200524
Concept code42357009
ValidityValid
ConceptStandard

Language	Synonym Concept
English	Disorder of digestive system specific to fetus OR newborn (disorder)
English	Disorder of digestive system specific to foetus OR newborn
English	Perinatal digestive system disorders
English	Perinatal disorder of digestive system
Spanish	trastorno del aparato digestivo específico del feto O recién nacido
Spanish	trastorno del aparato digestivo específico del feto O recién nacido (trastorno)
Spanish	trastorno perinatal del aparato digestivo

Valid start31-Jan-2002
Valid end31-Dec-2099

Term connections (198)

Relationship	Relates to	Concept id	Vocabulary
Active possibly_equivalent_to inactive (SNOMED)	Perinatal GIT disorder (& [ileus])	40357695	SNOMED
	[X]Digestive system disorders of fetus and newborn	44793962	SNOMED
	[X]Digestive system disorders of fetus and newborn	40399556	SNOMED
Active same_as inactive (SNOMED)	Perinatal GIT disorder (& [ileus])	40323031	SNOMED
Active was_a inactive (SNOMED)	Perinatal digestive system disorders NOS	3564855	SNOMED
	Perinatal digestive system disorders NOS	4049031	SNOMED
	Perinatal digestive system disorders NOS	40323034	SNOMED
	[X]Other specified perinatal digestive system disorders	44796731	SNOMED
	[X]Other specified perinatal digestive system disorders	40399560	SNOMED
Concept replaces	Specified perinatal disorder of digestive system, NEC	40315433	SNOMED
Has Module	SNOMED CT core	40642539	SNOMED
Has finding site (SNOMED)	Structure of digestive system	4314892	SNOMED
Has occurrence (SNOMED)	Fetal and/or neonatal period	37160324	SNOMED
	Fetal or neonatal period	42872435	SNOMED
Has status	Defined	40642537	SNOMED
Is a	Disorder of digestive system	4201745	SNOMED
	Disorder of fetus and/or newborn	441406	SNOMED
Non-standard to Standard map (OMOP)	Disorder of digestive system specific to fetus OR newborn	200524	SNOMED
Standard to Non-standard map (OMOP)	Congenital cirrhosis (machine translation)	1425065	ICD10CN
	Congenital cirrhosis (of liver)	45539251	ICD10CM
	Delayed passage of meconium (machine translation)	1425070	ICD10CN
	Disorder of digestive system specific to fetus OR newborn	200524	SNOMED
	Ileus - perinatal	3143056	Nebraska Lexicon
	Neonatal abdominal distension (machine translation)	1425064	ICD10CN
	Neonatal gallstones (machine translation)	1425063	ICD10CN
	Neonatal peptic ulcer (machine translation)	1425066	ICD10CN
	Other perinatal digestive system disorder NOS	3130764	Nebraska Lexicon
	Other perinatal digestive system disorder NOS	45480787	Read
	Other perinatal digestive system disorders	1425050	ICD10CN
	Other perinatal digestive system disorders	1572033	ICD10CM
	Other perinatal digestive system disorders	3130761	Nebraska Lexicon
	Other perinatal digestive system disorders	37092778	ICD10GM
	Other perinatal digestive system disorders	37612079	CIM10
	Other perinatal digestive system disorders	42495995	KCD7
	Other perinatal digestive system disorders	45510532	Read
	Other perinatal digestive system disorders	45592346	ICD10
	Other specified perinatal digestive system disorders	1425061	ICD10CN
	Other specified perinatal digestive system disorders	1425062	ICD10CN
	Other specified perinatal digestive system disorders	1572034	ICD10CM
	Other specified perinatal digestive system disorders	37092783	ICD10GM
	Other specified perinatal digestive system disorders	37614756	CIM10
	Other specified perinatal digestive system disorders	42496000	KCD7
	Other specified perinatal digestive system disorders	45577714	ICD10
	Other specified perinatal digestive system disorders	45592348	ICD10CM
	Other specified perinatal disorders of digestive system	44833910	ICD9CM
	Perinatal Disorder of Digestive System	45913921	CIEL
	Perinatal GIT disorder (& [ileus])	3107345	Nebraska Lexicon
	Perinatal GIT disorder (& [ileus])	40323031	SNOMED
	Perinatal GIT disorder (& [ileus])	40357695	SNOMED
	Perinatal digestive system disorder, unspecified	1425068	ICD10CN
	Perinatal digestive system disorder, unspecified	1425069	ICD10CN
	Perinatal digestive system disorder, unspecified	35210645	ICD10CM
	Perinatal digestive system disorder, unspecified	37092784	ICD10GM
	Perinatal digestive system disorder, unspecified	37612818	CIM10
	Perinatal digestive system disorder, unspecified	42496001	KCD7
	Perinatal digestive system disorder, unspecified	45601946	ICD10
	Perinatal digestive system disorders	45460551	Read
	Perinatal digestive system disorders NOS	3564855	SNOMED
	Perinatal digestive system disorders NOS	3107347	Nebraska Lexicon
	Perinatal digestive system disorders NOS	3130765	Nebraska Lexicon
	Perinatal digestive system disorders NOS	4049031	SNOMED
	Perinatal digestive system disorders NOS	40323034	SNOMED
	Perinatal digestive system disorders NOS	45507195	Read
	Perinatal disorder of digestive system	3241380	Nebraska Lexicon
	Perinatal disorders of digestive system	44826966	ICD9CM
	Specified Perinatal Disorder of Digestive System	45908358	CIEL
	Specified perinatal disorder of digestive system, NEC	40315433	SNOMED
	Specified perinatal disorder of digestive system, NEC -RETIRED-	3097756	Nebraska Lexicon
	Transient neonatal gastric volvulus (machine translation)	1425067	ICD10CN
	Unspecified perinatal disorder of digestive system	44831579	ICD9CM
	[X]Digestive system disorders of fetus and newborn	44793962	SNOMED
	[X]Digestive system disorders of fetus and newborn	45490670	Read
	[X]Other specified perinatal digestive system disorders	44796731	SNOMED
	[X]Other specified perinatal digestive system disorders	45474074	Read
	[X]Other specified perinatal digestive system disorders	40399560	SNOMED
Subsumes	Aberrant retro-esophageal subclavian artery causing dysphagia	4209546	SNOMED
	Alpha-1-antitrypsin deficiency	192275	SNOMED
	Alstrom syndrome	4270189	SNOMED
	Anterior maxillary protrusion, strabismus, intellectual disability syndrome	37163927	SNOMED
	Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome	37167984	SNOMED
	Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome	36716320	SNOMED
	Autosomal dominant hyperinsulinism due to SUR1 deficiency	37397032	SNOMED
	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency	37204850	SNOMED
	Autosomal recessive hyperinsulinism due to SUR1 deficiency	37204849	SNOMED
	Boder syndrome	37396384	SNOMED
	Carney Stratakis syndrome	36716386	SNOMED
	Cholestasis in newborn	4203366	SNOMED
	Chronic diarrhea due to glucoamylase deficiency	37396461	SNOMED
	Congenital achalasia of esophagus	45763775	SNOMED
	Congenital anomaly of digestive system	198249	SNOMED
	Congenital arteriovenous malformation of duodenum and jejunum	764974	SNOMED
	Congenital atrophy of left lobe of liver	4005461	SNOMED
	Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome	37166820	SNOMED
	Congenital chalasia of esophagus	36717148	SNOMED
	Congenital chronic diarrhea with protein-losing enteropathy	36676635	SNOMED
	Congenital disorder of gallbladder and biliary tract	196214	SNOMED
	Congenital diverticulitis of small intestine	36715867	SNOMED
	Congenital fecaliths causing obstruction	4071195	SNOMED
	Congenital functional disorders of the colon	443221	SNOMED
	Congenital functional disorders of the small intestine	4108884	SNOMED
	Congenital hiatus hernia	198246	SNOMED
	Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells	36717214	SNOMED
	Congenital malposition of tongue	760133	SNOMED
	Congenital monosaccharide malabsorption	42872854	SNOMED
	Congenital nasopharyngeal teratoma	604662	SNOMED
	Congenital palato-esophageal incoordination	4109783	SNOMED
	Congenital pyloric spasm	4005765	SNOMED
	Congenital secretory diarrhea	4093451	SNOMED
	Congenital velopharyngeal dysfunction	45763777	SNOMED
	Congenital viral hepatitis	4048592	SNOMED
	Contiguous ABCD1 DXS1357E deletion syndrome	36676512	SNOMED
	Crigler-Najjar syndrome, type I	4229773	SNOMED
	Deafness, small bowel diverticulosis, neuropathy syndrome	37116378	SNOMED
	Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency	37204835	SNOMED
	Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency	37204834	SNOMED
	Digenic hemochromatosis	1245328	SNOMED
	Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome	1075450	SNOMED
	Familial arthrogryposis-cholestatic hepatorenal syndrome	4265212	SNOMED
	Fetal cleft lip	37310907	SNOMED
	Fetal gastrointestinal abnormality	37310859	SNOMED
	Generalized congenital intestinal dysmotility	4109616	SNOMED
	Gingival fibromatosis with facial dysmorphism syndrome	36714449	SNOMED
	Glycogen phosphorylase kinase deficiency	4342778	SNOMED
	Glycogen storage disease, hepatic form	4246087	SNOMED
	Glycogen synthase deficiency	4031791	SNOMED
	Growth delay, intellectual disability, hepatopathy syndrome	37162089	SNOMED
	HELIX syndrome	37163592	SNOMED
	Harlequin fetus	4145173	SNOMED
	Heart defect, tongue hamartoma, polysyndactyly syndrome	37204832	SNOMED
	Hematemesis AND/OR melena due to swallowed maternal blood	201129	SNOMED
	Hepatic veno-occlusive disease with immunodeficiency syndrome	37110194	SNOMED
	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	35622780	SNOMED
	Hepatomphalocele	4278462	SNOMED
	Hereditary hemorrhagic telangiectasia of gingiva	37162654	SNOMED
	Hutchinson's teeth	4313730	SNOMED
	Hyperinsulinism and hyperammonemia syndrome	37397460	SNOMED
	Hyperinsulinism due to HNF1A deficiency	36715528	SNOMED
	Hyperinsulinism due to HNF4A deficiency	37397034	SNOMED
	Hyperinsulinism due to deficiency of glucokinase	37397139	SNOMED
	Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency	36715530	SNOMED
	Hyperinsulinism due to uncoupling protein 2 deficiency	36716024	SNOMED
	Hypoinsulinemic hypoglycemia and body hemihypertrophy	36676692	SNOMED
	Idiopathic transient neonatal hyperinsulinemia	4173187	SNOMED
	Intestinal enteropeptidase deficiency	4209713	SNOMED
	Intestinal lipofuscinosis	4151377	SNOMED
	Isolated neonatal sclerosing cholangitis	37163779	SNOMED
	Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia	607076	SNOMED
	Meconium peritonitis	4238980	SNOMED
	Median nodule of upper lip	36716142	SNOMED
	Mesenteric pregnancy	4113218	SNOMED
	Mitochondrial DNA depletion syndrome hepatocerebrorenal form	37204237	SNOMED
	Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency	37204828	SNOMED
	Monostotic fibrous dysplasia of periradicular alveolar bone	4001146	SNOMED
	Moon's molar teeth	4032996	SNOMED
	Mottled teeth, congenital	434069	SNOMED
	Mucopolysaccharidosis, MPS-II	4323827	SNOMED
	Mulberry molar teeth	37161176	SNOMED
	Natal tooth	4317521	SNOMED
	Navajo neurohepatopathy	37205068	SNOMED
	Necrotizing enterocolitis in fetus OR newborn	201957	SNOMED
	Neonatal disorder of oral mucosa	42537680	SNOMED
	Neonatal enamel hypoplasia	4025181	SNOMED
	Neonatal gastrointestinal disorder	4180181	SNOMED
	Neonatal hemorrhage of liver	42536722	SNOMED
	Neonatal hepatitis	4320490	SNOMED
	Neonatal hepatocellular damage	4318835	SNOMED
	Neonatal hepatosplenomegaly	4214373	SNOMED
	Neonatal hypotonia of hypopharynx	36716745	SNOMED
	Neonatal mass of hypopharynx	36716886	SNOMED
	Neonatal melena	4048608	SNOMED
	Neonatal oral candidiasis	42538263	SNOMED
	Neonatal tooth	4243198	SNOMED
	Newborn ingestion of maternal blood	4079846	SNOMED
	Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome	37118954	SNOMED
	Oculootodental syndrome	36674947	SNOMED
	Omphalocele with obstruction	4035782	SNOMED
	Pancreatic colipase deficiency	4290254	SNOMED
	Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome	36716259	SNOMED
	Pancreatic triacylglycerol lipase deficiency	4302604	SNOMED
	Perinatal disorders of liver and/or biliary system	4173179	SNOMED
	Perinatal gastrointestinal hemorrhage	194158	SNOMED
	Perinatal gastrointestinal perforation in preterm infant	1245922	SNOMED
	Perinatal intestinal obstruction	4171091	SNOMED
	Perinatal intestinal perforation	199925	SNOMED
	Perinatal melena	4048282	SNOMED
	Periodontal Ehlers-Danlos syndrome	4176273	SNOMED
	Peutz-Jeghers syndrome	4182399	SNOMED
	Primary copper-associated hepatitis	42575779	SNOMED Veterinary
	Rotor syndrome	4139925	SNOMED
	Schmitt Gillenwater Kelly syndrome	37396323	SNOMED
	Shwachman syndrome	4232178	SNOMED
	Synthetic defect of bile acids	4340395	SNOMED
	Transient neonatal hypoglycemia due to hyperinsulinemia	42536567	SNOMED
	Vitelline anomaly of small intestine	42597124	SNOMED Veterinary
	X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome	37110165	SNOMED
	XTE syndrome	4323123	SNOMED
	[X]Digestive system disorders of fetus and newborn	44793962	SNOMED
	[X]Other specified perinatal digestive system disorders	44796731	SNOMED

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Definitions

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Details

Term connections (198)

Athena – OHDSI Vocabularies Repository

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