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Rh deficiency syndrome
1 OMIM reference -
3 associated genes
8 connected diseases
No signs/symptoms info
Disease Type of connection
Overhydrated hereditary stomatocytosis
Hereditary spherocytosis
8p11.2 deletion syndrome
Transaldolase deficiency
Williams syndrome
Autosomal dominant distal renal tubular acidosis
Distal renal tubular acidosis with anemia
Southeast Asian ovalocytosis
Synonym(s):
- Rh-null syndrome
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: unknown
Average age onset: no data available
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
RHAG Q02094180297
RHCE P18577111700
RHD Q02161111680
No signs/symptoms info available.