retinitis pigmentosa 19
retinitis pigmentosa that has material basis in mutation in the ABCA4 gene on chromosome 1p22
Press Enter · cited answer in seconds
0 sources
retinitis pigmentosa 19
Summary
retinitis pigmentosa 19 is a rare disease[1].
Key Facts
- retinitis pigmentosa 19's instance of is recorded as rare disease[2].
- retinitis pigmentosa 19's instance of is recorded as class of disease[3].
- retinitis pigmentosa 19's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 19's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 19's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 19's MeSH descriptor ID is recorded as C566637[7].
- retinitis pigmentosa 19's OMIM ID is recorded as 601718[8].
- retinitis pigmentosa 19's Disease Ontology ID is recorded as DOID:0110354[9].
- retinitis pigmentosa 19's genetic association is recorded as ABCA4[10].
- retinitis pigmentosa 19's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110354[11].
- retinitis pigmentosa 19's exact match is recorded as http://identifiers.org/doid/DOID:0110354[12].
- retinitis pigmentosa 19's UMLS CUI is recorded as C1866422[13].
- retinitis pigmentosa 19's ICD-10-CM is recorded as H35.5[14].
- retinitis pigmentosa 19's GARD rare disease ID is recorded as 10398[15].
- retinitis pigmentosa 19's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- retinitis pigmentosa 19's Mondo ID is recorded as MONDO_0011137[17].
- retinitis pigmentosa 19's UniProt disease ID is recorded as DI-00985[18].