rickets, X-Linked hypophosphatemic

Preferred Label : rickets, X-Linked hypophosphatemic;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0577258;

UMLS CUI

C3540852;

Automatic exact mappings (from CISMeF team)
- X-linked Hypophosphatemic Rickets [NCIt concept]
Currated CISMeF NLP mapping
- Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder) [SNOMED CT concept]
- Hypophosphatemic rickets, X-linked recessive [OMIM Phenotype]
- X-Linked Dominant Hypophosphatemic Rickets [NCIt concept]
- X-linked dominant hypophosphatemic rickets [DO Concept]
- X-linked hypophosphatemia [ORDO Disease]
Related record
- familial hypophosphatemic rickets [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- X-Linked Dominant Hypophosphatemic Rickets [NCIt concept]
- X-linked Hypophosphatemic Rickets [NCIt concept]
- X-linked hypophosphataemia [MedDRA LLT]
- X-linked hypophosphatemia [MedDRA LLT]