Hypophosphatemic bone disease

Preferred Label : Hypophosphatemic bone disease;

Symbol : HBD;

CISMeF acronym : HBD;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant; ? heterogeneous;

Prefixed ID : %146350;

Details

Origin ID

146350;

UMLS CUI

C1840321;

Currated CISMeF NLP mapping
- hypophosphatemic bone disease [MeSH concept]
- hypophosphatemic bone disease [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bowing of the legs [HPO term]
- Hypophosphatemia [HPO term]
- Osteomalacia [HPO term]
- Rickets [HPO term]
- Short stature [HPO term]
- Skeletal dysplasia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hypophosphatemic bone disease [MeSH Supplementary Concept]
- hypophosphatemic bone disease [MeSH concept]

Keyword's position in hierarchy(ies) :

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