hypertension, Early-Onset, autosomal dominant, with severe exacerbation in pregnancy

Preferred Label : hypertension, Early-Onset, autosomal dominant, with severe exacerbation in pregnancy;

Origin ID

C565359;

UMLS CUI

C1854631;

Currated CISMeF NLP mapping
- Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy [OMIM Phenotype]
MeSH term(s) associated for indexing
- hypertension [MeSH Descriptor]
Record concept(s)
- hypertension, Early-Onset, autosomal dominant, with severe exacerbation in pregnancy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypertension due to gain-of-function mutations in the mineralocorticoid receptor [ORDO Disease]
- Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy [OMIM Phenotype]