robinson miller bensimon syndrome

Preferred Label : robinson miller bensimon syndrome;

MeSH note : Familial ectodermal dysplasia with sensori-neural deafness and other anomalies;

MeSH synonym : deafness and onychodystrophy, dominant form;

Details

Origin ID

C535864;

UMLS CUI

C2931049;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant deafness-onychodystrophy syndrome [ORDO Disease]
- Deafness – onychodystrophy, autosomal dominant [ICD-11 More detail]
MeSH term(s) associated for indexing
- ectodermal dysplasia [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- Robinson Miller Bensimon syndrome [MeSH concept]
See also (suggested by CISMeF)
- deafness, congenital onychodystrophy, recessive form [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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