Leber congenital amaurosis 7
Leber congenital amaurosis that has material basis in mutation in the CRX gene on chromosome 19q13
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Leber congenital amaurosis 7
Summary
Leber congenital amaurosis 7 is a rare disease[1].
Key Facts
- Leber congenital amaurosis 7's instance of is recorded as rare disease[2].
- Leber congenital amaurosis 7's instance of is recorded as class of disease[3].
- Leber congenital amaurosis 7 is a type of Leber congenital amaurosis[4].
- Leber congenital amaurosis 7 is a type of genetic disease[5].
- Leber congenital amaurosis 7 is a type of monogenic disease[6].
- Leber congenital amaurosis 7's genetic association is recorded as CRX[7].
- Leber congenital amaurosis 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110333[8].
- Leber congenital amaurosis 7's exact match is recorded as http://identifiers.org/doid/DOID:0110333[9].
- Leber congenital amaurosis 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].