hypophosphatemic rickets, X-Linked dominant

Preferred Label : hypophosphatemic rickets, X-Linked dominant;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0010917;

UMLS CUI

C0733682;

Broader MeSH concept(s)
- rickets, hypophosphatemic [MeSH concept]
Currated CISMeF NLP mapping
- Hypophosphatemic rickets, X-linked dominant [OMIM Phenotype]
- X-Linked Dominant Hypophosphatemic Rickets [NCIt concept]
- X-linked dominant hypophosphatemic rickets [DO Concept]
Related record
- familial hypophosphatemic rickets [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypophosphatemic rickets, X-linked dominant [OMIM Phenotype]
- X-Linked Dominant Hypophosphatemic Rickets [NCIt concept]