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BioAssay Ontology
Last uploaded:
February 21, 2024
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| Preferred Name | Alagille syndrome | |
| Synonyms |
Alagille-Watson syndrome Arteriohepatic dysplasia |
|
| Definitions |
A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts. OMIM mapping confirmed by DO. [SN]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_9245 |
|
| comment |
OMIM mapping confirmed by DO. [SN].
|
|
| database_cross_reference |
MESH:D016738 UMLS_CUI:C0085280 ICD10CM:Q44.7 OMIM:118450 SNOMEDCT_US_2020_03_01:31742004 OMIM:610205 GARD:804 NCI:C35139 ORDO:52
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| has exact match |
MESH:D016738
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|
| has exact synonym |
Alagille-Watson syndrome Arteriohepatic dysplasia
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|
| has_obo_namespace |
disease_ontology
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|
| id |
DOID:9245
|
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| imported from | ||
| in_subset | ||
| label |
Alagille syndrome
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|
| notation |
DOID:9245
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|
| prefLabel |
Alagille syndrome
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|
| textual definition |
A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts.
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|
| subClassOf |
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