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Items: 2

1.

Autosomal dominant nonsyndromic hearing loss 31

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 6p21.3. [from MONDO]

MedGen UID:
325209
Concept ID:
C1837617
Disease or Syndrome
2.

Old-aged sensorineural hearing impairment

Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process. [from NCI]

MedGen UID:
10911
Concept ID:
C0033074
Pathologic Function

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