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loading...| Preferred Name |
Nonsyndromic sensorineural hearing loss |
|
| Synonyms |
Deafness, nonsyndromic sensorineural, mitochondrial |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C537845 |
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| altLabel |
Deafness, nonsyndromic sensorineural, mitochondrial Autosomal dominant nonsyndromic hereditary hearing impairment Nonsyndromic hereditary hearing impairment |
|
| cui |
C3151897 C1842137 |
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| HM |
D006319 |
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| Inverse of RB |
0 |
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| Mapped to | ||
| MDA |
20100825 |
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| MeSH Frequency |
123 |
|
| MMR |
20160719 |
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| notation |
C537845 |
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| prefLabel |
Nonsyndromic sensorineural hearing loss |
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| SC |
3 |
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| 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 |
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| TERMUI |
T000904066 T743952 T743953 T743954 |
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| TH |
OMIM (2013) ORD (2010) |
|
| tui |
T047 T033 |
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