hypophosphatemic rickets, autosomal recessive, 2

Preferred Label : hypophosphatemic rickets, autosomal recessive, 2;

MeSH note : mutations in ENPP1;

Origin ID

C567647;

UMLS CUI

C2750078;

Currated CISMeF NLP mapping
- Hypophosphatemic rickets, autosomal recessive, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- familial hypophosphatemic rickets [MeSH Descriptor]
Record concept(s)
- hypophosphatemic rickets, autosomal recessive, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypophosphatemic rickets, autosomal recessive, 2 [OMIM Phenotype]