ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal recessive distal renal tubular acidosis without deafness

Hyperlipidemia type 3


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ATP6V0A4	(0.63)	APOE

Citations in the biomedical literature:

Autosomal recessive distal renal tubular acidosis without deafness		Hyperlipidemia type 3
	Synonym(s): - AR dRTA without deafness - AR dRTA without hearing loss - Autosomal recessive distal renal tubular acidosis without hearing loss - Renal tubular acidosis type 1c		Synonym(s): - Broad-betalipoproteinemia - Dyslipidemia type 3 - Familial dysbetalipoproteinemia - Familial hyperlipoproteinemia type 3 - HLP type 3 - Hyperlipoproteinemia type 3 - Remnant disease

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare genetic disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: normal Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: D006952

No signs/symptoms info available.