arteriohepatic dysplasia

Preferred Label : arteriohepatic dysplasia;

Détails

Origin ID

D4-01203;

UMLS CUI

C0085280;

Automatic exact mappings (from CISMeF team)
- Alagille syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- Alagille Syndrome [NCIt concept]
- Alagille syndrome [DO Concept]
- Alagille syndrome [MedDRA Preferred Term]
- Alagille syndrome [ORDO Disease]
- Alagille syndrome 1 [OMIM Phenotype]
- Arteriohepatic dysplasia [PASCAL descriptor]
- Arteriohepatic dysplasia (disorder) [SNOMED CT concept]
- Other congenital malformations of liver [ICD-10 Sub-category]
- Other congenital malformations of liver [ICD-10 Sub-category (who)]
- alagille syndrome [MeSH Descriptor]
- alagille syndrome [MeSH concept]
ICD-10 exact mapping(s)
- Other congenital malformations of liver [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic biliary tract disease [ORDO Disease]
- Polymalformative genetic syndrome with increased risk of developing cancer [ORDO Disease]
- Rare biliary tract disease [ORDO Disease]
- Rare disease with glaucoma as a major feature [ORDO Disease]
- Rare syndrome with cardiac malformations [ORDO Disease]
- Syndromic developmental defect of the eye [ORDO Disease]
- Syndromic renal or urinary tract malformation [ORDO Disease]
- Syndromic visceral malformation [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Arteriohepatic dysplasia (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Alagille Syndrome [NCIt concept]
- Alagille syndrome [ORDO Disease]
- Alagille syndrome [Disease (Nov.)]
- Alagille syndrome [DO Concept]
- Alagille syndrome [MedDRA Preferred Term]
- Arteriohepatic dysplasia (disorder) [SNOMED CT concept]
- Other congenital malformations of liver [ICD-10 Sub-category (who)]
- alagille syndrome [MeSH Descriptor]
- alagille syndrome [MeSH concept]

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