Deafness, unilateral, with delayed endolymphatic hydrops

Preferred Label : Deafness, unilateral, with delayed endolymphatic hydrops;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %612097;

Details

Origin ID

612097;

UMLS CUI

C2677512;

Automatic exact mappings (from CISMeF team)
- Non-syndromic genetic deafness [ORDO Disease]
Currated CISMeF NLP mapping
- deafness, unilateral, with delayed endolymphatic hydrops [MeSH concept]
- deafness, unilateral, with delayed endolymphatic hydrops [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Edema [HPO term]
- Unilateral deafness [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- deafness, unilateral, with delayed endolymphatic hydrops [MeSH Supplementary Concept]
- deafness, unilateral, with delayed endolymphatic hydrops [MeSH concept]

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