ODCs

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

PROTEIN INTERACTIONS: 1

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

Rh deficiency syndrome

Autosomal dominant distal renal tubular acidosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RHAG	(0.52)	SLC4A1

Citations in the biomedical literature:

Rh deficiency syndrome		Autosomal dominant distal renal tubular acidosis
	Synonym(s): - Rh-null syndrome		Synonym(s): - AD dRTA - Renal tubular acidosis type 1a

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: Class of prevalence: unknown Average age onset: no data available Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.