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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Autosomal dominant distal renal tubular acidosis
Rh deficiency syndrome

SLC4A1 RHAG
RHCE
RHD


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Autosomal dominant distal renal tubular acidosis
SLC4A1
Rh deficiency syndrome
RHAG RHCE RHD



Autosomal dominant distal renal tubular acidosis
Rh deficiency syndrome

Synonym(s):
- AD dRTA
- Renal tubular acidosis type 1a

Synonym(s):
- Rh-null syndrome

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

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

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

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

No signs/symptoms info available.