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Hearing loss, sensorineural, autosomal-mitochondrial type

MedGen UID:
346566
Concept ID:
C1857332
Disease or Syndrome
Synonym: Deafness, sensorineural, autosomal-mitochondrial type
 
Monarch Initiative: MONDO:0009090
OMIM®: 221745

Clinical features

From HPO
Sensorineural hearing loss disorder
MedGen UID:
9164
Concept ID:
C0018784
Disease or Syndrome
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.
Progressive sensorineural hearing impairment
MedGen UID:
335894
Concept ID:
C1843156
Disease or Syndrome
A progressive form of sensorineural hearing impairment.

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