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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Chronic myelomonocytic leukemia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

ETV6 TNK2
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
(0.63)
TNK2



Citations in the biomedical literature:


Chronic myelomonocytic leukemia
ETV6 PDGFRB
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
TNK2



Chronic myelomonocytic leukemia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
1 MeSH reference: D015477
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.