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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pseudohypoaldosteronism type 2C
Familial atrial myxoma

WNK1 PRKAR1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WNK1
(0.63)
PRKAR1A



Citations in the biomedical literature:


Pseudohypoaldosteronism type 2C
WNK1
Familial atrial myxoma
PRKAR1A



Pseudohypoaldosteronism type 2C
Familial atrial myxoma

Synonym(s):
- PHA2C

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538262

No signs/symptoms info available.