Corneal degeneration, ribbonlike, with deafness

Preferred Label : Corneal degeneration, ribbonlike, with deafness;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Band keratopathy with deafness;

Inheritance : Autosomal dominant;

Prefixed ID : 121450;

Details

Origin ID

121450;

UMLS CUI

C1852556;

Currated CISMeF NLP mapping
- corneal degeneration, ribbonlike, with deafness [MeSH concept]
- corneal degeneration, ribbonlike, with deafness [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Band keratopathy [HPO term]
- Hearing impairment [HPO term]
- Ribbonlike corneal degeneration [HPO term]
- Ribbonlike corneal degeneration [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- corneal degeneration, ribbonlike, with deafness [MeSH Supplementary Concept]
- corneal degeneration, ribbonlike, with deafness [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients