ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Gitelman syndrome

Pseudohypoaldosteronism type 2D

CLCNKB	(UniProt - OMIM)		KLHL3	(UniProt - OMIM)
SLC12A3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC12A3	(0.63)	KLHL3

Citations in the biomedical literature:

Gitelman syndrome		Pseudohypoaldosteronism type 2D
	Synonym(s): - Primary renal tubular hypokalemic hypomagnesemia with hypocalciuria		Synonym(s): - PHA2D

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		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 - 1 MeSH reference: D053579		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.