nephronophthisis 9
nephronophthisis that has material basis in homozygous mutation in the NEK8 gene on chromosome 17q11
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nephronophthisis 9
Summary
nephronophthisis 9 is a rare disease[1].
Key Facts
- nephronophthisis 9's instance of is recorded as rare disease[2].
- nephronophthisis 9's instance of is recorded as class of disease[3].
- nephronophthisis 9's subclass of is recorded as nephronophthisis[4].
- nephronophthisis 9's OMIM ID is recorded as 613824[5].
- nephronophthisis 9's OMIM ID is recorded as 613824[6].
- nephronophthisis 9's Disease Ontology ID is recorded as DOID:0111120[7].
- nephronophthisis 9's genetic association is recorded as NEK8[8].
- nephronophthisis 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111120[9].
- nephronophthisis 9's exact match is recorded as http://identifiers.org/doid/DOID:0111120[10].
- nephronophthisis 9's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_655[11].
- nephronophthisis 9's UMLS CUI is recorded as C3151188[12].
- nephronophthisis 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- nephronophthisis 9's Mondo ID is recorded as MONDO_0013444[14].
- nephronophthisis 9's UniProt disease ID is recorded as DI-03050[15].