retinitis pigmentosa 48
retinitis pigmentosa that has material basis in mutation in the GUCA1B gene on chromosome 6p21.1
Press Enter · cited answer in seconds
0 sources
retinitis pigmentosa 48
Summary
retinitis pigmentosa 48 is a rare disease[1].
Key Facts
- retinitis pigmentosa 48's instance of is recorded as rare disease[2].
- retinitis pigmentosa 48's instance of is recorded as class of disease[3].
- retinitis pigmentosa 48's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 48's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 48's OMIM ID is recorded as 613827[6].
- retinitis pigmentosa 48's Disease Ontology ID is recorded as DOID:0110382[7].
- retinitis pigmentosa 48's genetic association is recorded as GUCA1B[8].
- retinitis pigmentosa 48's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110382[9].
- retinitis pigmentosa 48's exact match is recorded as http://identifiers.org/doid/DOID:0110382[10].
- retinitis pigmentosa 48's UMLS CUI is recorded as C3151190[11].
- retinitis pigmentosa 48's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 48's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 48's Mondo ID is recorded as MONDO_0013447[14].
- retinitis pigmentosa 48's UniProt disease ID is recorded as DI-03035[15].