Leber congenital amaurosis 11
Leber congenital amaurosis that has material basis in mutation n the IMPDH1 gene on chromosome 7q31.3-q32
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Leber congenital amaurosis 11
Summary
Leber congenital amaurosis 11 is a rare disease[1].
Key Facts
- Leber congenital amaurosis 11's instance of is recorded as rare disease[2].
- Leber congenital amaurosis 11's instance of is recorded as class of disease[3].
- Leber congenital amaurosis 11 is a type of Leber congenital amaurosis[4].
- Leber congenital amaurosis 11 is a type of genetic disease[5].
- Leber congenital amaurosis 11 is a type of autosomal dominant disease[6].
- Leber congenital amaurosis 11's genetic association is recorded as IMPDH1[7].
- Leber congenital amaurosis 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110216[8].
- Leber congenital amaurosis 11's exact match is recorded as http://identifiers.org/doid/DOID:0110216[9].
- Leber congenital amaurosis 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].