cone-rod dystrophy 19
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24
Press Enter · cited answer in seconds
0 sources
cone-rod dystrophy 19
Summary
cone-rod dystrophy 19 is a rare disease[1].
Key Facts
- cone-rod dystrophy 19's instance of is recorded as rare disease[2].
- cone-rod dystrophy 19's instance of is recorded as class of disease[3].
- cone-rod dystrophy 19's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 19's OMIM ID is recorded as 615860[5].
- cone-rod dystrophy 19's Disease Ontology ID is recorded as DOID:0111025[6].
- cone-rod dystrophy 19's genetic association is recorded as TTLL5[7].
- cone-rod dystrophy 19's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111025[8].
- cone-rod dystrophy 19's exact match is recorded as http://identifiers.org/doid/DOID:0111025[9].
- cone-rod dystrophy 19's UMLS CUI is recorded as C4014501[10].
- cone-rod dystrophy 19's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- cone-rod dystrophy 19's Mondo ID is recorded as MONDO_0014372[12].
- cone-rod dystrophy 19's UniProt disease ID is recorded as DI-04129[13].