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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 5
1 OMIM reference -
5 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Juvenile myelomonocytic leukemia

CACNG2 CBL
CDH15 KRAS
CTNNB1 NF1
DOCK8 NRAS
DYNC1H1 PTPN11
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
CTNNB1
GRIN2B
GRIN1
DYNC1H1
(0.72)
(0.65)
(0.62)
(0.59)
(0.14)
PTPN11
CBL
PTPN11
NF1
NF1



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11



Autosomal dominant nonsyndromic intellectual deficit
Juvenile myelomonocytic leukemia

Synonym(s):
(no synonyms)

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
13 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D054429

No signs/symptoms info available.