Atresia of external auditory canal and conductive deafness

Preferred Label : Atresia of external auditory canal and conductive deafness;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %108760;

Details

Origin ID

108760;

UMLS CUI

C3502361;

Automatic exact mappings (from CISMeF team)
- External auditory canal aplasia/hypoplasia [ORDO Disease]
- atresia of external auditory canal and conduction deafness [MeSH concept]
- external auditory canal, bilateral atresia of, with congenital vertical talus [MeSH Supplementary Concept]
HPO term(s)
- Aplasia/Hypoplasia of the middle ear [HPO term]
- Atresia of the external auditory canal [HPO term]
- Autosomal dominant inheritance [HPO term]
- Conductive hearing impairment [HPO term]
- Delayed pneumatization of the mastoid process [HPO term]
- External auditory canal stenosis/atresia [HPO term]
- Stenosis of the external auditory canal [HPO term]
ORDO concept(s)
- External auditory canal aplasia/hypoplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atresia of external auditory canal and conduction deafness [MeSH concept]

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