achromatopsia 7
achromatopsia that has material basis in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23
Press Enter · cited answer in seconds
0 sources
achromatopsia 7
Summary
achromatopsia 7 is a class of disease[1].
Key Facts
- achromatopsia 7's instance of is recorded as class of disease[2].
- achromatopsia 7's subclass of is recorded as achromatopsia[3].
- achromatopsia 7's subclass of is recorded as autosomal recessive disease[4].
- achromatopsia 7's OMIM ID is recorded as 616517[5].
- achromatopsia 7's Disease Ontology ID is recorded as DOID:0110009[6].
- achromatopsia 7's genetic association is recorded as ATF6[7].
- achromatopsia 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110009[8].
- achromatopsia 7's exact match is recorded as http://identifiers.org/doid/DOID:0110009[9].
- achromatopsia 7's UMLS CUI is recorded as C4225297[10].
- achromatopsia 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- achromatopsia 7's Mondo ID is recorded as MONDO_0014677[12].
- achromatopsia 7's UniProt disease ID is recorded as DI-04499[13].