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Overhydrated hereditary stomatocytosis
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Rh deficiency syndrome
Hereditary spherocytosis
8p11.2 deletion syndrome
Autosomal dominant distal renal tubular acidosis
Distal renal tubular acidosis with anemia
Southeast Asian ovalocytosis
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
RHAG Q02094180297
No signs/symptoms info available.