Disorder of digestive system specific to fetus OR newborn

Code	`42357009`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20190131

311808009Aberrant retro-esophageal subclavian artery causing dysphagia disorder

720980004Alopecia, psychomotor epilepsy, periodontal pyorrhoea, intellectual disability syndrome disorder

30188007Alpha-1-antitrypsin deficiency disorder

63702009Alstrom syndrome disorder

1222706005Anterior maxillary protrusion, strabismus, intellectual disability syndrome disorder

1269271003Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome disorder

722288007Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome disorder

717046003Autosomal dominant hyperinsulinism due to SUR1 deficiency disorder

716180009Boder syndrome disorder

722377004Carney Stratakis syndrome disorder

433237003Cholestasis in newborn disorder

716277000Chronic diarrhoea due to glucoamylase deficiency disorder

702364003Chylomicron retention disease disorder

700283004Congenital achalasia of oesophagus disorder

69518005Congenital anomaly of digestive system disorder

204788008Congenital atrophy of left lobe of liver disorder

1260140008Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome disorder

721154006Congenital chalasia of oesophagus disorder

773579007Congenital chronic diarrhoea with protein-losing enteropathy disorder

235913009Congenital disorder of gallbladder and biliary tract disorder

721646008Congenital diverticulitis of small intestine disorder

253778009Congenital functional disorders of the colon disorder

253767001Congenital functional disorders of the small intestine disorder

206372007Congenital hepatitis disorder

47028006Congenital hiatus hernia disorder

722392003Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells disorder

450849003Congenital monosaccharide malabsorption disorder

1003468008Congenital nasopharyngeal teratoma disorder

253758001Congenital palato-oesophageal incoordination disorder

204670005Congenital pyloric spasm disorder

25898005Congenital secretory diarrhoea disorder

198273008Congenital vaginal enterocele disorder

700285006Congenital velopharyngeal dysfunction disorder

773415005Contiguous ABCD1 DXS1357E deletion syndrome disorder

8933000Crigler-Najjar syndrome, type I disorder

733071009Deafness, small bowel diverticulosis, neuropathy syndrome disorder

783741006Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency disorder

783740007Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency disorder

1299153008Digenic haemochromatosis disorder

1304114004Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome disorder

62216007Familial arthrogryposis-cholestatic hepatorenal syndrome disorder

121801000119105Fetal gastrointestinal abnormality disorder

253785008Generalised congenital intestinal dysmotility disorder

719687007Gingival fibromatosis with facial dysmorphism syndrome disorder

235908005Glycogen phosphorylase kinase deficiency disorder

6075009Glycogen storage disease, hepatic form disorder

237964009Glycogen synthase deficiency disorder

1186713004Growth delay, intellectual disability, hepatopathy syndrome disorder

1217380005HELIX syndrome disorder

783738002Heart defect, tongue hamartoma, polysyndactyly syndrome disorder

724361001Hepatic veno-occlusive disease with immunodeficiency syndrome disorder

764962002Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 disorder

36631002Hepatomphalocele disorder

1197033002Hereditary haemorrhagic telangiectasia of gingiva disorder

718106009Hyperinsulinism and hyperammonaemia syndrome disorder

717182006Hyperinsulinism due to deficiency of glucokinase disorder

721236002Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency disorder

721834007Hyperinsulinism due to uncoupling protein 2 deficiency disorder

773666007Hypoinsulinemic hypoglycaemia and body hemihypertrophy disorder

276563006Idiopathic transient neonatal hyperinsulinaemia disorder

56661000Intestinal enteropeptidase deficiency disorder

28212002Intestinal lipofuscinosis disorder

1220580006Isolated neonatal sclerosing cholangitis disorder

1149069001Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia disorder

57341009Meconium peritonitis disorder

782771007Mitochondrial DNA depletion syndrome hepatocerebrorenal form disorder

783734000Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency disorder

109714003Monostotic fibrous dysplasia of periradicular alveolar bone disorder

84752003Mottled teeth, congenital disorder

70737009Mucopolysaccharidosis, MPS-II disorder

1177081002Mulberry molar teeth disorder

21995002Natal tooth disorder

784346006Navajo neurohepatopathy disorder

2707005Necrotising enterocolitis in foetus OR newborn disorder

737211006Neonatal disorder of oral mucosa disorder

196279002Neonatal enamel hypoplasia disorder

363219007Neonatal gastrointestinal disorder disorder

735677007Neonatal haemorrhage of liver disorder

69800000Neonatal hepatitis disorder

95555006Neonatal hepatocellular damage disorder

80378000Neonatal hepatosplenomegaly disorder

722916005Neonatal hypotonia of hypopharynx disorder

717155003Neonatal intrahepatic cholestasis due to citrin deficiency disorder

723111007Neonatal mass of hypopharynx disorder

206424005Neonatal melaena disorder

746223006Neonatal oral candidiasis disorder

58748004Neonatal tooth disorder

723442008Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome disorder

770944002Oculootodental syndrome disorder

1542009Omphalocele with obstruction disorder

69478001Pancreatic colipase deficiency disorder

722207000Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome disorder

78960005Pancreatic triacylglycerol lipase deficiency disorder

276548008Perinatal disorders of liver and/or biliary system disorder

48729005Perinatal gastrointestinal haemorrhage disorder

1854871000000103Perinatal gastrointestinal perforation in preterm infant disorder

276521007Perinatal intestinal obstruction disorder

65390006Perinatal intestinal perforation disorder

206407004Perinatal melaena disorder

50869007Periodontal Ehlers-Danlos syndrome disorder

54411001Peutz-Jeghers syndrome disorder

717053007Renal tubulopathy with encephalopathy and liver failure syndrome disorder

32891000Rotor syndrome disorder

206565007Rumination in newborn disorder

716092007Schmitt Gillenwater Kelly syndrome disorder

89454001Shwachman syndrome disorder

235915002Synthetic defect of bile acids disorder

735496003Transient neonatal hypoglycaemia due to hyperinsulinaemia disorder

724276006X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome disorder

7037003XTE syndrome disorder

Disorder of digestive system specific to fetus OR newborn

Synonyms

Parents (2)

Children (110)