Format

Send to:

Choose Destination

Links from PubMed

Hyperaldosteronism, familial, type II(HALD2)

MedGen UID:
340137
Concept ID:
C1854107
Disease or Syndrome
Synonyms: FH II; HALD2
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
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

Diagnosis

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

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center