Mitochondrially Inherited Nonsyndromic Sensorineural Deafness

Preferred Label : Mitochondrially Inherited Nonsyndromic Sensorineural Deafness;

NCIt definition : A maternally inherited form of nonsyndromic sensorineural deafness that is caused by a mutation in any of several mitochondrial genes.;

NCI Metathesaurus CUI : CL550972;

Details

Origin ID

C148321;

UMLS CUI

C4724974;

Has associated anatomic sites
- Ear [NCIt concept]
- Head and Neck [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

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