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Pseudohypoaldosteronism type 2C
1 OMIM reference -
1 associated gene
39 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary sensory and autonomic neuropathy type 2
Pseudohypoaldosteronism type 2D
Distal myopathy with posterior leg and anterior hand involvement
Muscle filaminopathy
17p13.3 microduplication syndrome
Acrodysostosis with multiple hormone resistance
Acute megakaryoblastic leukemia without Down syndrome
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Cardiofaciocutaneous syndrome
Carney complex
Cree leukoencephalopathy
Cystic fibrosis
Distal 17p13.3 microdeletion syndrome
Early infantile epileptic encephalopathy
Familial atrial myxoma
Familial isolated dilated cardiomyopathy
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Infantile cerebellar-retinal degeneration
Inflammatory myofibroblastic tumor
Juvenile autosomal recessive medullary cystic kidney disease
Kearns-Sayre syndrome
Miller-Dieker syndrome
Muscular dystrophy, Selcen type
Primary pigmented nodular adrenocortical disease
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 1
Translocation renal cell carcinoma
Cowden syndrome
Proteus syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive primary microcephaly
Peters anomaly
Seckel syndrome

Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
WNK1 Q9H4A3605232
No signs/symptoms info available.