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loading...| Preferred Name |
Gilbert Syndrome |
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| Synonyms |
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| Definitions |
An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C84729 |
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| code |
C84729 |
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| Contributing_Source |
GDC |
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| definition |
An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice. |
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| in_subset | ||
| Is_Value_For_GDC_Property | ||
| label |
Gilbert Syndrome |
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| Maps_To |
Gilbert's Syndrome |
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| Preferred_Name |
Gilbert Syndrome |
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| prefixIRI |
NCIT:C84729 |
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| prefLabel |
Gilbert Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0017551 |
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| subClassOf |
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