congenital stationary night blindness autosomal dominant 3
congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21
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congenital stationary night blindness autosomal dominant 3
Summary
congenital stationary night blindness autosomal dominant 3 is a rare disease[1].
Key Facts
- congenital stationary night blindness autosomal dominant 3's instance of is recorded as rare disease[2].
- congenital stationary night blindness autosomal dominant 3's instance of is recorded as class of disease[3].
- congenital stationary night blindness autosomal dominant 3 is a type of congenital stationary night blindness[4].
- congenital stationary night blindness autosomal dominant 3 is a type of hereditary retinal dystrophy[5].
- congenital stationary night blindness autosomal dominant 3 is a type of genetic disease[6].
- congenital stationary night blindness autosomal dominant 3 is a type of autosomal dominant disease[7].
- congenital stationary night blindness autosomal dominant 3's genetic association is recorded as GNAT1[8].
- congenital stationary night blindness autosomal dominant 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110715[9].
- congenital stationary night blindness autosomal dominant 3's exact match is recorded as http://identifiers.org/doid/DOID:0110715[10].
- congenital stationary night blindness autosomal dominant 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].