retinitis pigmentosa 7
retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21
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retinitis pigmentosa 7
Summary
retinitis pigmentosa 7 is a rare disease[1].
Key Facts
- retinitis pigmentosa 7's instance of is recorded as rare disease[2].
- retinitis pigmentosa 7's instance of is recorded as class of disease[3].
- retinitis pigmentosa 7's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 7's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 7's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 7's subclass of is recorded as digenic disease[7].
- retinitis pigmentosa 7's subclass of is recorded as autosomal dominant disease[8].
- retinitis pigmentosa 7's OMIM ID is recorded as 608133[9].
- retinitis pigmentosa 7's Disease Ontology ID is recorded as DOID:0110383[10].
- retinitis pigmentosa 7's genetic association is recorded as ROM1[11].
- retinitis pigmentosa 7's genetic association is recorded as PRPH2[12].
- retinitis pigmentosa 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110383[13].
- retinitis pigmentosa 7's exact match is recorded as http://identifiers.org/doid/DOID:0110383[14].
- retinitis pigmentosa 7's UMLS CUI is recorded as C1842475[15].
- retinitis pigmentosa 7's UMLS CUI is recorded as C2675553[16].
- retinitis pigmentosa 7's UMLS CUI is recorded as C2675552[17].
- retinitis pigmentosa 7's ICD-10-CM is recorded as H35.5[18].
- retinitis pigmentosa 7's GARD rare disease ID is recorded as 10386[19].
- retinitis pigmentosa 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- retinitis pigmentosa 7's Mondo ID is recorded as MONDO_0011974[21].
- retinitis pigmentosa 7's UniProt disease ID is recorded as DI-00975[22].