achromatopsia 3
achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2
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achromatopsia 3
Summary
achromatopsia 3 is a class of disease[1].
Key Facts
- achromatopsia 3's instance of is recorded as class of disease[2].
- achromatopsia 3's subclass of is recorded as achromatopsia[3].
- achromatopsia 3's subclass of is recorded as autosomal recessive disease[4].
- achromatopsia 3's OMIM ID is recorded as 262300[5].
- achromatopsia 3's Disease Ontology ID is recorded as DOID:0110008[6].
- achromatopsia 3's genetic association is recorded as CNGB3[7].
- achromatopsia 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110008[8].
- achromatopsia 3's exact match is recorded as http://identifiers.org/doid/DOID:0110008[9].
- achromatopsia 3's UMLS CUI is recorded as C1849792[10].
- achromatopsia 3's GARD rare disease ID is recorded as 9650[11].
- achromatopsia 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- achromatopsia 3's Mondo ID is recorded as MONDO_0009875[13].
- achromatopsia 3's UniProt disease ID is recorded as DI-00023[14].