hypophosphatemic rickets with hypercalciuria, hereditary

Preferred Label : hypophosphatemic rickets with hypercalciuria, hereditary;

MeSH synonym : hypercalciuric rickets;

Details

Origin ID

C562793;

UMLS CUI

C1853271;

Currated CISMeF NLP mapping
- Autosomal dominant hypophosphatemic bone disease (disorder) [SNOMED CT concept]
- Autosomal recessive hypophosphatemic bone disease (disorder) [SNOMED CT concept]
- Hereditary Hypophosphatemic Rickets with Hypercalciuria [NCIt concept]
- Hereditary hypophosphatemic rickets with hypercalciuria [ORDO Disease]
- Hereditary hypophosphatemic rickets with hypercalciuria (disorder) [SNOMED CT concept]
- Hypophosphatemic rickets with hypercalciuria, hereditary [OMIM Phenotype]
- hereditary hypophosphatemic rickets with hypercalciuria [DO Concept]
- hereditary hypophosphatemic rickets with hypercalciuria [Disease (Nov.)]
MeSH term(s) associated for indexing
- familial hypophosphatemic rickets [MeSH Descriptor]
- hypercalciuria [MeSH Descriptor]
Record concept(s)
- hypophosphatemic rickets with hypercalciuria, hereditary [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive hypophosphatemic bone disease (disorder) [SNOMED CT concept]
- Hereditary Hypophosphatemic Rickets with Hypercalciuria [NCIt concept]
- Hereditary hypophosphatemic rickets with hypercalciuria [ORDO Disease]
- Hereditary hypophosphatemic rickets with hypercalciuria (disorder) [SNOMED CT concept]
- Hypophosphatemic rickets with hypercalciuria, hereditary [OMIM Phenotype]
- hereditary hypophosphatemic rickets with hypercalciuria [DO Concept]
- hereditary hypophosphatemic rickets with hypercalciuria [Disease (Nov.)]

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