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Items: 2

1.

Hearing loss, autosomal dominant 73

MedGen UID:
1627153
Concept ID:
C4540024
Disease or Syndrome
2.

Autosomal recessive nonsyndromic hearing loss 84A

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PTPRQ gene. [from MONDO]

MedGen UID:
462004
Concept ID:
C3150654
Disease or Syndrome

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