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Hyperaldosteronism, familial, type II(HALD2)

MedGen UID:
Concept ID:
Disease or Syndrome
Synonyms: FH II; HALD2
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
Concept ID:
Intellectual Product
Sources: HPO, OMIM, Orphanet
Autosomal dominant inheritance refers to genetic conditions that occur when a mutation is present in one copy of a given gene (i.e., the person is heterozygous).
Autosomal dominant inheritance (HPO, OMIM, Orphanet)
OMIM®: 605635
Orphanet: ORPHA404

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
Follow this link to review classifications for Hyperaldosteronism, familial, type II in Orphanet.

Recent clinical studies


Simonetti GD, Mohaupt MG, Bianchetti MG
Eur J Pediatr 2012 Oct;171(10):1433-9. Epub 2011 Mar 15 doi: 10.1007/s00431-011-1440-7. PMID: 21404100

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