Ossicular malformations, familial

Preferred Label : Ossicular malformations, familial;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 165680;

Details

Origin ID

165680;

UMLS CUI

C1833790;

Currated CISMeF NLP mapping
- Ossicular Malformations, familial [MeSH concept]
- ossicular malformations, familial [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the middle ear ossicles [HPO term]
- Autosomal dominant inheritance [HPO term]
- Congenital conductive hearing impairment [HPO term]
- Malformed ossicles [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ossicular Malformations, familial [MeSH concept]
- ossicular malformations, familial [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients