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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
HPO: HP:0007692

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVNonnuclear polymorphic congenital cataract

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