Hyperparathyroidism, primary, caused by water clear cell hyperplasia

Preferred Label : Hyperparathyroidism, primary, caused by water clear cell hyperplasia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 600166;

Details

Origin ID

600166;

UMLS CUI

C1838501;

Automatic exact mappings (from CISMeF team)
- Primary parathyroid hyperplasia [ORDO Disease]
Currated CISMeF NLP mapping
- hyperparathyroidism, primary, caused by water clear cell hyperplasia [MeSH concept]
- hyperparathyroidism, primary, caused by water clear cell hyperplasia [MeSH Supplementary Concept]
DO Cross reference
- primary hyperparathyroidism [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Primary hyperparathyroidism [HPO term]
ORDO concept(s)
- Familial isolated hyperparathyroidism [ORDO Disease]
- Primary parathyroid hyperplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperparathyroidism, primary, caused by water clear cell hyperplasia [MeSH Supplementary Concept]
- hyperparathyroidism, primary, caused by water clear cell hyperplasia [MeSH concept]

Keyword's position in hierarchy(ies) :

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