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Isolated delta-storage pool disease
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Familial platelet syndrome with predisposition to acute myelogenous leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Isolated delta-storage pool disease
Familial platelet syndrome with predisposition to acute myelogenous leukemia

FLI1
(UniProt - OMIM)
 RUNX1
(UniProt - OMIM)
RUNX1
(UniProt - OMIM)

COMMON
GENES 		RUNX1


Citations in the biomedical literature:


Isolated delta-storage pool disease
FLI1 RUNX1
Familial platelet syndrome with predisposition to acute myelogenous leukemia



Isolated delta-storage pool disease
Familial platelet syndrome with predisposition to acute myelogenous leukemia

Synonym(s):
- Isolated delta-SPD
- Isolated dense-SPD
- Isolated dense-storage pool disease
Synonym(s):
- FPD/AML syndrome
- FPS/AML syndrome
- Familial platelet disorder with associated myeloid malignancy
- Familial platelet syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: no data available
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.