retinitis pigmentosa 73
retinitis pigmentosa that has material basis in mutation in the HGSNAT gene on chromosome 8p11
Press Enter · cited answer in seconds
0 sources
retinitis pigmentosa 73
Summary
retinitis pigmentosa 73 is a rare disease[1].
Key Facts
- retinitis pigmentosa 73's instance of is recorded as rare disease[2].
- retinitis pigmentosa 73's instance of is recorded as class of disease[3].
- retinitis pigmentosa 73's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 73's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 73's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 73's OMIM ID is recorded as 616544[7].
- retinitis pigmentosa 73's Disease Ontology ID is recorded as DOID:0110389[8].
- retinitis pigmentosa 73's genetic association is recorded as HGSNAT[9].
- retinitis pigmentosa 73's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110389[10].
- retinitis pigmentosa 73's exact match is recorded as http://identifiers.org/doid/DOID:0110389[11].
- retinitis pigmentosa 73's UMLS CUI is recorded as C4225287[12].
- retinitis pigmentosa 73's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 73's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- retinitis pigmentosa 73's Mondo ID is recorded as MONDO_0014687[15].
- retinitis pigmentosa 73's UniProt disease ID is recorded as DI-04519[16].