cone-rod dystrophy 11
cone-rod dystrophy that has material basis in heterozygous mutation in the RAX2 gene on chromosome 19p13
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cone-rod dystrophy 11
Summary
cone-rod dystrophy 11 is a rare disease[1].
Key Facts
- cone-rod dystrophy 11's instance of is recorded as rare disease[2].
- cone-rod dystrophy 11's instance of is recorded as class of disease[3].
- cone-rod dystrophy 11's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 11's MeSH descriptor ID is recorded as C563671[5].
- cone-rod dystrophy 11's OMIM ID is recorded as 610381[6].
- cone-rod dystrophy 11's OMIM ID is recorded as 610381[7].
- cone-rod dystrophy 11's Disease Ontology ID is recorded as DOID:0111018[8].
- cone-rod dystrophy 11's genetic association is recorded as RAX2[9].
- cone-rod dystrophy 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111018[10].
- cone-rod dystrophy 11's exact match is recorded as http://identifiers.org/doid/DOID:0111018[11].
- cone-rod dystrophy 11's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1872[12].
- cone-rod dystrophy 11's UMLS CUI is recorded as C1835865[13].
- cone-rod dystrophy 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- cone-rod dystrophy 11's Mondo ID is recorded as MONDO_0012483[15].
- cone-rod dystrophy 11's UniProt disease ID is recorded as DI-00325[16].