polycystic kidney disease 2
autosomal dominant polycystic kidney disease that has material basis in autosomal dominant inheritance of mutation in the PKD2 gene on chromosome 4q22.1
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polycystic kidney disease 2
Summary
polycystic kidney disease 2 is a rare disease[1].
Key Facts
- polycystic kidney disease 2's instance of is recorded as rare disease[2].
- polycystic kidney disease 2's instance of is recorded as class of disease[3].
- polycystic kidney disease 2's subclass of is recorded as autosomal dominant polycystic kidney disease[4].
- polycystic kidney disease 2's OMIM ID is recorded as 613095[5].
- polycystic kidney disease 2's OMIM ID is recorded as 613095[6].
- polycystic kidney disease 2's Disease Ontology ID is recorded as DOID:0110859[7].
- polycystic kidney disease 2's Orphanet ID is recorded as 730[8].
- polycystic kidney disease 2's genetic association is recorded as PKD2[9].
- polycystic kidney disease 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110859[10].
- polycystic kidney disease 2's exact match is recorded as http://identifiers.org/doid/DOID:0110859[11].
- polycystic kidney disease 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_730[12].
- polycystic kidney disease 2's UMLS CUI is recorded as C2751306[13].
- polycystic kidney disease 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- polycystic kidney disease 2's Mondo ID is recorded as MONDO_0013131[15].
- polycystic kidney disease 2's UniProt disease ID is recorded as DI-00926[16].