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Items: 3

1.

Autosomal recessive nonsyndromic hearing loss 1A

Nonsyndromic hearing loss and deafness (DFNB1) is characterized by congenital non-progressive mild-to-profound sensorineural hearing impairment. No other associated medical findings are present. [from GeneReviews]

MedGen UID:
388720
Concept ID:
C2673759
Disease or Syndrome
2.

Deafness, digenic, GJB2/GJB3

MedGen UID:
382183
Concept ID:
C2673761
Disease or Syndrome
3.

Deafness, digenic, GJB2/GJB6

MedGen UID:
382182
Concept ID:
C2673760
Disease or Syndrome
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