cone-rod dystrophy 9
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the ADAM9 gene on chromosome 8p11
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cone-rod dystrophy 9
Summary
cone-rod dystrophy 9 is a rare disease[1].
Key Facts
- cone-rod dystrophy 9's instance of is recorded as rare disease[2].
- cone-rod dystrophy 9's instance of is recorded as class of disease[3].
- cone-rod dystrophy 9's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 9's OMIM ID is recorded as 612775[5].
- cone-rod dystrophy 9's Disease Ontology ID is recorded as DOID:0111020[6].
- cone-rod dystrophy 9's genetic association is recorded as ADAM9[7].
- cone-rod dystrophy 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111020[8].
- cone-rod dystrophy 9's exact match is recorded as http://identifiers.org/doid/DOID:0111020[9].
- cone-rod dystrophy 9's UMLS CUI is recorded as C1423873[10].
- cone-rod dystrophy 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- cone-rod dystrophy 9's Mondo ID is recorded as MONDO_0013002[12].
- cone-rod dystrophy 9's UniProt disease ID is recorded as DI-02490[13].