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Nonnuclear polymorphic congenital cataract(PCC)

MedGen UID:
854886
•Concept ID:
C3888391
•
Congenital Abnormality; Disease or Syndrome
Synonyms: CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL; PCC
 
OMIM®: 115700

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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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