Ribbing disease

Preferred Label : Ribbing disease;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Diaphyseal sclerosis, multiple;

Inheritance : Autosomal recessive;

Prefixed ID : 601477;

Details

Origin ID

601477;

UMLS CUI

C1832273;

Currated CISMeF NLP mapping
- Ribbing disease [MeSH concept]
- ribbing disease [MeSH Supplementary Concept]
HPO term(s)
- Adolescent onset [HPO term]
- Autosomal recessive inheritance [HPO term]
- Diaphyseal sclerosis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ribbing disease [MeSH concept]
- ribbing disease [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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