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loading...| Preferred Name |
Congenital Hepatic Fibrosis |
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| Synonyms |
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| Definitions |
A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C97071 |
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| code |
C97071 |
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| Contributing_Source |
Cellosaurus |
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| definition |
A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts. |
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| in_subset | ||
| label |
Congenital Hepatic Fibrosis |
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| Preferred_Name |
Congenital Hepatic Fibrosis |
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| prefixIRI |
NCIT:C97071 |
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| prefLabel |
Congenital Hepatic Fibrosis |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0009714 |
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| subClassOf |
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