Hyperparathyroidism 3

Preferred Label : Hyperparathyroidism 3;

Symbol : HRPT3;

CISMeF acronym : HRPT3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of familial isolated hyperparathyroidism, see HRPT1 (145000).;

Prefixed ID : %610071;

Details

Origin ID

610071;

UMLS CUI

C1864729;

Automatic exact mappings (from CISMeF team)
- Hereditary Isolated Hyperparathyroidism [NCIt concept]
- hyperparathyroidism 1 [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- hyperparathyroidism 3 [MeSH concept]
- hyperparathyroidism 3 [MeSH Supplementary Concept]
DO Cross reference
- hyperparathyroidism [DO Concept]
ORDO concept(s)
- Familial isolated hyperparathyroidism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial isolated hyperparathyroidism [ORDO Disease]
- hyperparathyroidism 3 [MeSH Supplementary Concept]
- hyperparathyroidism 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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