Autosomal dominant non-nuclear cataract

MedGen UID:: 318648
•Concept ID:: C1832526
•: Congenital Abnormality

Synonyms:	Autosomal dominant nonnuclear polymorphic congenital cataract; Cataract congenital dominant non nuclear; Cataract, Nonnuclear Polymorphic Congenital, Autosomal Dominant; Cataract, polymorphic congenital

Monarch Initiative:	MONDO:0022673

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Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35.

Rogaev EI, Rogaeva EA, Korovaitseva GI, Farrer LA, Petrin AN, Keryanov SA, Turaeva S, Chumakov I, St George-Hyslop P, Ginter EK
Hum Mol Genet 1996 May;5(5):699-703. doi: 10.1093/hmg/5.5.699. PMID: 8733140

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