Hyperaldosteronism, familial type 1
Common Name(s)
Hyperaldosteronism, familial type 1
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hyperaldosteronism, familial type 1" for support, advocacy or research.
How do you compare to others with this condition?
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hyperaldosteronism, familial type 1" for support, advocacy or research.
Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Hyperaldosteronism, familial type 1 can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Scientific Literature
Articles from the PubMed Database
Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hyperaldosteronism, familial type 1" returned 0 free, full-text research articles on human participants.
No free, full-text research articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Hyperaldosteronism, familial type 1".
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hyperaldosteronism, familial type 1" returned 0 free, full-text review articles on human participants.
No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Hyperaldosteronism, familial type 1".
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/condition/familial-porencephaly
https://ghr.nlm.nih.gov/condition/optic-atrophy-type-1
https://ghr.nlm.nih.gov/condition/distal-arthrogryposis-type-1
https://ghr.nlm.nih.gov/condition/type-1-diabetes
https://ghr.nlm.nih.gov/condition/atelosteogenesis-type-1
https://ghr.nlm.nih.gov/condition/neurofibromatosis-type-1
https://ghr.nlm.nih.gov/condition/otopalatodigital-syndrome-type-1
https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-1
https://ghr.nlm.nih.gov/condition/pseudohypoaldosteronism-type-1
https://ghr.nlm.nih.gov/condition/familial-dysautonomia
https://ghr.nlm.nih.gov/condition/aicardi-goutieres-syndrome
https://ghr.nlm.nih.gov/gene/CYP11B1
https://ghr.nlm.nih.gov/gene/CYP11B2
https://ghr.nlm.nih.gov/condition/acute-necrotizing-encephalopathy-type-1
https://ghr.nlm.nih.gov/condition/liddle-syndrome
https://ghr.nlm.nih.gov/condition/familial-lipoprotein-lipase-deficiency
https://ghr.nlm.nih.gov/condition/leukocyte-adhesion-deficiency-type-1
https://ghr.nlm.nih.gov/condition/aldosterone-producing-adenoma
https://ghr.nlm.nih.gov/gene/KCNJ5
There are currently no related results available in GeneReviews.
There are currently no related results available in Genetic Testing Registry.
Clinical Trial Information This information is provided by ClinicalTrials.gov
There are currently no open clinical trials for this condition.
Finding the right clinical trial for Hyperaldosteronism, familial type 1 can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.