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Paris-Trousseau thrombocytopenia
1 OMIM reference -
1 associated gene
31 connected diseases
2 signs/symptoms
Disease Type of connection
Ewing sarcoma
Extraskeletal Ewing sarcoma
Peripheral primitive neuroectodermal tumor
Isolated delta-storage pool disease
Acute basophilic leukemia
Beta-thalassemia - X-linked thrombocytopenia
Congenital erythropoietic porphyria
Thrombocytopenia with congenital dyserythropoietic anemia
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Chronic myelomonocytic leukemia
Congenital dyserythropoietic anemia type IV
Congenital mesoblastic nephroma
Fibrosarcoma
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Precursor B-cell acute lymphoblastic leukemia
Familial pancreatic carcinoma
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Heritable pulmonary arterial hypertension
Alternating hemiplegia of childhood
Aneurysm - osteoarthritis syndrome
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss
Familial thoracic aortic aneurysm and aortic dissection
Rapid-onset dystonia-parkinsonism
Desmoplastic small round cell tumor
Extraskeletal myxoid chondrosarcoma
Melanoma of soft part
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- 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:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C538617
Gene symbol UniProt reference OMIM reference
FLI1 Q01543193067
Frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Structural anomalies of the cardio-circulatory system