Nephrolithiasis-Osteoporosis, hypophosphatemic, 1

Preferred Label : Nephrolithiasis-Osteoporosis, hypophosphatemic, 1;

MeSH note : mutation in SLC34A1;

MeSH synonym : NPHLOP1;

Origin ID

C567363;

UMLS CUI

C2676786;

Currated CISMeF NLP mapping
- Nephrolithiasis/osteoporosis, hypophosphatemic, 1 [OMIM Phenotype]
- hypophosphatemic nephrolithiasis/osteoporosis 1 [DO Concept]
DO Cross reference
- hypophosphatemic nephrolithiasis/osteoporosis 1 [DO Concept]
MeSH term(s) associated for indexing
- hypophosphatemia [MeSH Descriptor]
- nephrolithiasis [MeSH Descriptor]
- osteoporosis [MeSH Descriptor]
- renal tubular transport, inborn errors [MeSH Descriptor]
Record concept(s)
- Nephrolithiasis-Osteoporosis, hypophosphatemic, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nephrolithiasis/osteoporosis, hypophosphatemic, 1 [OMIM Phenotype]
- hypophosphatemic nephrolithiasis/osteoporosis 1 [DO Concept]