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Items: 2

1.

Autosomal dominant nonsyndromic hearing loss 22

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. [from MONDO]

MedGen UID:
419894
Concept ID:
C2931767
Disease or Syndrome
2.

Autosomal recessive nonsyndromic hearing loss 37

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. [from MONDO]

MedGen UID:
375076
Concept ID:
C1843028
Disease or Syndrome

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