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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
13 OMIM references -
14 associated genes
No signs/symptoms info
Chronic myelomonocytic leukemia
Autosomal dominant nonsyndromic intellectual deficit

ETV6 CACNG2
PDGFRB CDH15
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
(0.55)
SYNGAP1



Citations in the biomedical literature:


Chronic myelomonocytic leukemia
ETV6 PDGFRB
Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4



Chronic myelomonocytic leukemia
Autosomal dominant nonsyndromic intellectual deficit

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.