pseudohypoparathyroidism type 2

Preferred Label : pseudohypoparathyroidism type 2;

MeSH synonym : php ii; Php2; pseudohypoparathyroidism, type ii;

Origin ID

C548077;

UMLS CUI

C2932717;

Automatic exact mappings (from CISMeF team)
- ASAH1 wt Allele [NCIt concept]
- PHP [OMIConto metadata]
- Pseudohypoparathyroidism type 2 [ICD-11 More detail]
- Pseudohypoparathyroidism type II (disorder) [SNOMED CT concept]
- Pseudohypoparathyroidism, type II [OMIM Phenotype]
- SRY-box transcription factor 3 [ORDO Gene]
- Secondary Parathyroid Hormone Resistance [NCIt concept]
- pseudohypoparathyroidism type i a [SNOMED Notion]
- pseudohypoparathyroidism type i b [SNOMED Notion]
Currated CISMeF NLP mapping
- Pseudohypoparathyroidism type 2 [ORDO Disease]
MeSH term(s) associated for indexing
- pseudohypoparathyroidism [MeSH Descriptor]
ORDO relation(s)
- Pseudohypoparathyroidism type 2 [ORDO Disease]
Record concept(s)
- Pseudohypoparathyroidism Type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pseudohypoparathyroidism type 2 [ORDO Disease]
- Pseudohypoparathyroidism type II (disorder) [SNOMED CT concept]
- Pseudohypoparathyroidism, type II [OMIM Phenotype]
- Secondary Parathyroid Hormone Resistance [NCIt concept]