• USHER SYNDROME, TYPE ID/F, DIGENIC
  USHER SYNDROME, TYPE ID/F, DIGENIC
  MedGen
• C3276419[conceptid] (1)
  MedGen
• "ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A, AUTOSOMAL DOMINANT"[Di... (2)
  "ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A, AUTOSOMAL DOMINANT"[Disease/phenotype] AND "OMIM"[submitter]

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  ClinVar
• C0751161[trait identifier] AND "OMIM"[submitter] (13)
  ClinVar
• "UCP3 POLYMORPHISM, EXON 6 SPLICE DONOR JUNCTION"[Disease/phenoty... (1)
  "UCP3 POLYMORPHISM, EXON 6 SPLICE DONOR JUNCTION"[Disease/phenotype] AND "OMIM"[submitter]

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  ClinVar

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