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Pseudohypoaldosteronism type 2D
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Pseudohypoaldosteronism type 2B
Pseudohypoaldosteronism type 2E
Hereditary sensory and autonomic neuropathy type 2
Pseudohypoaldosteronism type 2C
Gitelman syndrome
Early infantile epileptic encephalopathy
Synonym(s):
- PHA2D
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KLHL3 Q9UH77605775
No signs/symptoms info available.