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Items: 6

1.

Nonsyndromic Deafness

MedGen UID:
777982
Concept ID:
C3711374
Disease or Syndrome
2.

Deafness

An inherited or acquired condition characterized by the inability to hear in one or both ears. [from NCI]

MedGen UID:
4155
Concept ID:
C0011053
Finding; Finding
3.

Hearing impairment

A decreased magnitude of the sensory perception of sound. [from HPO]

MedGen UID:
235586
Concept ID:
C1384666
Disease or Syndrome
4.

Hearing loss

A partial or complete loss of hearing in one or both ears. It is classified as conductive, sensory, or central. [from NCI]

MedGen UID:
854601
Concept ID:
C3887873
Finding
5.

Autosomal recessive nonsyndromic hearing loss 63

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

MedGen UID:
409872
Concept ID:
C1969621
Disease or Syndrome
6.

Disorder of ear

A non-neoplastic or neoplastic disorder that affects the ear. Representative examples include infections, hearing disorders, benign neoplasms, and carcinomas. [from NCI]

MedGen UID:
3946
Concept ID:
C0013447
Disease or Syndrome
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