Leber congenital amaurosis 12
Leber congenital amaurosis that has material basis in mutation in the RD3 gene on chromosome 1q32
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Summary
Leber congenital amaurosis 12 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: Leber congenital amaurosis[4], genetic disease[5], autosomal recessive disease[6]
- Genetic association: RD3[7]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110080[8], http://identifiers.org/doid/DOID:0110080[9]
- On focus list of Wikimedia project: WikiProject Medicine[10]