retinitis pigmentosa 51
retinitis pigmentosa that has material basis in mutation in the TTC8 gene on chromosome 14q31
Press Enter · cited answer in seconds
0 sources
Summary
retinitis pigmentosa 51 is a rare disease[1].
Key Facts
- retinitis pigmentosa 51's instance of is recorded as rare disease[2].
- retinitis pigmentosa 51's instance of is recorded as class of disease[3].
- retinitis pigmentosa 51's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 51's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 51's OMIM ID is recorded as 613464[6].
- retinitis pigmentosa 51's Disease Ontology ID is recorded as DOID:0110398[7].
- retinitis pigmentosa 51's genetic association is recorded as TTC8[8].
- retinitis pigmentosa 51's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110398[9].
- retinitis pigmentosa 51's exact match is recorded as http://identifiers.org/doid/DOID:0110398[10].
- retinitis pigmentosa 51's UMLS CUI is recorded as C3150715[11].
- retinitis pigmentosa 51's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 51's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 51's Mondo ID is recorded as MONDO_0013274[14].
- retinitis pigmentosa 51's UniProt disease ID is recorded as DI-02707[15].