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Paris-Trousseau thrombocytopenia
1 OMIM reference -
1 associated gene
2 signs/symptoms
PROTEIN INTERACTIONS: 1
Hereditary persistence of fetal hemoglobin - sickle cell disease
4 associated genes
No signs/symptoms info
Paris-Trousseau thrombocytopenia
Hereditary persistence of fetal hemoglobin - sickle cell disease

FLI1
(UniProt - OMIM)
 HBB
(UniProt - OMIM)
HBG1
(UniProt - OMIM)
HBG2
(UniProt - OMIM)
KLF1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLI1
(0.79)
KLF1


Citations in the biomedical literature:


Paris-Trousseau thrombocytopenia
FLI1
Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1



Paris-Trousseau thrombocytopenia
Hereditary persistence of fetal hemoglobin - sickle cell disease

Synonym(s):
(no synonyms)

Synonym(s):
- HPFH - sickle cell disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare hematologic disease
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 -
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: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C538617
External references:
No OMIM references
No MeSH references
Paris-Trousseau thrombocytopenia

Frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Structural anomalies of the cardio-circulatory system



Hereditary persistence of fetal hemoglobin - sickle cell disease

(no data available)