ODCs

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2 OMIM references -
3 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Infantile Bartter syndrome with deafness

Gitelman syndrome

Citations in the biomedical literature:

Infantile Bartter syndrome with deafness		Gitelman syndrome
	Synonym(s): - Bartter syndrome type 4		Synonym(s): - Primary renal tubular hypokalemic hypomagnesemia with hypocalciuria

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D053579

No signs/symptoms info available.