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CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT(PCC)

MedGen UID:
318648
Concept ID:
C1832526
Congenital Abnormality; Disease or Syndrome
Synonyms: Autosomal dominant nonnuclear polymorphic congenital cataract; Cataract congenital dominant non nuclear; Cataract, Nonnuclear Polymorphic Congenital, Autosomal Dominant; Cataract, polymorphic congenital
 
OMIM®: 601286

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