ODCs

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4 OMIM references -
5 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

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

Hereditary spherocytosis

Autosomal dominant distal renal tubular acidosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ANK1 EPB42	(0.83) (0.63)	SLC4A1 SLC4A1

Citations in the biomedical literature:

Hereditary spherocytosis		Autosomal dominant distal renal tubular acidosis
	Synonym(s): - Minkowski-Chauffard disease		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: 1-5 / 10 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant

	External references: 4 OMIM references - 2 MeSH references: C536356 / D013103		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.