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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Hemimegalencephaly
Chronic myelomonocytic leukemia

AKT3 ETV6
PIK3CA PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PIK3CA
(0.52)
PDGFRB



Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
Chronic myelomonocytic leukemia
ETV6 PDGFRB



Hemimegalencephaly
Chronic myelomonocytic leukemia

Synonym(s):
- Unilateral megalencephaly

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.