cone-rod dystrophy 15
cone-rod dystrophy that has material basis in homozygous mutation in the CDHR1 gene on chromosome 10q23
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cone-rod dystrophy 15
Summary
cone-rod dystrophy 15 is a rare disease[1].
Key Facts
- cone-rod dystrophy 15's instance of is recorded as rare disease[2].
- cone-rod dystrophy 15's instance of is recorded as class of disease[3].
- cone-rod dystrophy 15's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 15's OMIM ID is recorded as 613660[5].
- cone-rod dystrophy 15's OMIM ID is recorded as 613660[6].
- cone-rod dystrophy 15's Disease Ontology ID is recorded as DOID:0111021[7].
- cone-rod dystrophy 15's genetic association is recorded as CDHR1[8].
- cone-rod dystrophy 15's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111021[9].
- cone-rod dystrophy 15's exact match is recorded as http://identifiers.org/doid/DOID:0111021[10].
- cone-rod dystrophy 15's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1872[11].
- cone-rod dystrophy 15's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_791[12].
- cone-rod dystrophy 15's UMLS CUI is recorded as C3150912[13].
- cone-rod dystrophy 15's UMLS CUI is recorded as C3552852[14].
- cone-rod dystrophy 15's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- cone-rod dystrophy 15's Mondo ID is recorded as MONDO_0013348[16].
- cone-rod dystrophy 15's UniProt disease ID is recorded as DI-02944[17].