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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
Synonym(s):
(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.