cone-rod dystrophy 13
cone-rod dystrophy that has material basis in mutation in the RPGRIP1 gene on chromosome 14q11.2
Press Enter · cited answer in seconds
0 sources
cone-rod dystrophy 13
Summary
cone-rod dystrophy 13 is a rare disease[1].
Key Facts
- cone-rod dystrophy 13's instance of is recorded as rare disease[2].
- cone-rod dystrophy 13's instance of is recorded as class of disease[3].
- cone-rod dystrophy 13's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 13's MeSH descriptor ID is recorded as C567698[5].
- cone-rod dystrophy 13's OMIM ID is recorded as 608194[6].
- cone-rod dystrophy 13's Disease Ontology ID is recorded as DOID:0111016[7].
- cone-rod dystrophy 13's genetic association is recorded as RPGRIP1[8].
- cone-rod dystrophy 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111016[9].
- cone-rod dystrophy 13's exact match is recorded as http://identifiers.org/doid/DOID:0111016[10].
- cone-rod dystrophy 13's UMLS CUI is recorded as C2750720[11].
- cone-rod dystrophy 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- cone-rod dystrophy 13's Mondo ID is recorded as MONDO_0011987[13].
- cone-rod dystrophy 13's UniProt disease ID is recorded as DI-00323[14].