cone-rod dystrophy 18
cone-rod dystrophy that has material basis in homozygous mutation in the RAB28 gene on chromosome 4p15
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cone-rod dystrophy 18
Summary
cone-rod dystrophy 18 is a rare disease[1].
Key Facts
- cone-rod dystrophy 18's instance of is recorded as rare disease[2].
- cone-rod dystrophy 18's instance of is recorded as class of disease[3].
- cone-rod dystrophy 18's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 18's OMIM ID is recorded as 615374[5].
- cone-rod dystrophy 18's OMIM ID is recorded as 615374[6].
- cone-rod dystrophy 18's Disease Ontology ID is recorded as DOID:0111024[7].
- cone-rod dystrophy 18's genetic association is recorded as RAB28[8].
- cone-rod dystrophy 18's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111024[9].
- cone-rod dystrophy 18's exact match is recorded as http://identifiers.org/doid/DOID:0111024[10].
- cone-rod dystrophy 18's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1872[11].
- cone-rod dystrophy 18's UMLS CUI is recorded as C3809299[12].
- cone-rod dystrophy 18's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- cone-rod dystrophy 18's Mondo ID is recorded as MONDO_0014153[14].
- cone-rod dystrophy 18's UniProt disease ID is recorded as DI-03861[15].