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Items: 2

1.

Autosomal recessive nonsyndromic hearing loss 21

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

MedGen UID:
355030
Concept ID:
C1863655
Disease or Syndrome
2.

Autosomal dominant nonsyndromic hearing loss 12

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

MedGen UID:
321902
Concept ID:
C1832187
Disease or Syndrome

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