| Preferred Name |
Nonsyndromic sensorineural hearing loss |
| Synonyms |
Nonsyndromic hereditary hearing impairment |
| ID |
http://purl.bioontology.org/ontology/MESH/C537845 |
| altLabel |
Nonsyndromic hereditary hearing impairment Autosomal dominant nonsyndromic hereditary hearing impairment Deafness, nonsyndromic sensorineural, mitochondrial |
| cui |
C3151897 C1842137 |
| HM |
D006319 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20100825 |
| MeSH Frequency |
123 |
| MMR |
20160719 |
| notation |
C537845 |
| prefLabel |
Nonsyndromic sensorineural hearing loss |
| SC |
3 |
| Scope Statement |
Partial or total loss of hearing that is not associated with other signs and symptoms. Some hereditary cases may be caused by mutations in MITOCHONDRIAL GENES. OMIM: 500008 |
| TERMUI |
T743952 T743954 T000904066 T743953 |
| TH |
ORD (2010) OMIM (2013) |
| tui |
T033 T047 |