hypophosphatemic rickets, autosomal dominant

Preferred Label : hypophosphatemic rickets, autosomal dominant;

MeSH note : mutation in FGF23;

MeSH synonym : vitamin D-Resistant rickets, autosomal dominant; hypophosphatemia, autosomal dominant;

Is substance : O;

Détails

Origin ID

C562791;

UMLS CUI

C0342642;

Currated CISMeF NLP mapping
- Autosomal Dominant Hypophosphatemia Rickets [NCIt concept]
- Autosomal dominant hypophosphataemic rickets [ICD-11 More detail]
- Autosomal dominant hypophosphataemic rickets [MedDRA LLT]
- Autosomal dominant hypophosphatemic rickets [ORDO Disease]
- Autosomal dominant hypophosphatemic rickets [MedDRA LLT]
- Autosomal dominant hypophosphatemic rickets (disorder) [SNOMED CT concept]
- Hypophosphatemic rickets [HPO term]
- Hypophosphatemic rickets [MedDRA LLT]
- Hypophosphatemic rickets, autosomal dominant [OMIM Phenotype]
- autosomal dominant hypophosphatemic rickets [DO Concept]
- autosomal dominant hypophosphatemic rickets [Disease (Nov.)]
MeSH term(s) associated for indexing
- familial hypophosphatemic rickets [MeSH Descriptor]
- rickets [MeSH Descriptor]
Record concept(s)
- hypophosphatemic rickets, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal Dominant Hypophosphatemia Rickets [NCIt concept]
- Autosomal dominant hypophosphataemic rickets [MedDRA LLT]
- Autosomal dominant hypophosphatemic rickets [MedDRA LLT]
- Autosomal dominant hypophosphatemic rickets (disorder) [SNOMED CT concept]
- Hypophosphatemic rickets, autosomal dominant [OMIM Phenotype]
- autosomal dominant hypophosphatemic rickets [DO Concept]
- autosomal dominant hypophosphatemic rickets [Disease (Nov.)]

Position du mot-clé dans l'(les) arborescence(s) :

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