hyperparathyroidism, neonatal Self-Limited primary, with hypercalciuria

Preferred Label : hyperparathyroidism, neonatal Self-Limited primary, with hypercalciuria;

Origin ID

C565496;

UMLS CUI

C1855924;

Currated CISMeF NLP mapping
- Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperparathyroidism, primary [MeSH Descriptor]
Record concept(s)
- hyperparathyroidism, neonatal Self-Limited primary, with hypercalciuria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria [OMIM Phenotype]