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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile myelomonocytic leukemia
Lethal congenital contracture syndrome type 2

CBL ERBB3
KRAS
NF1
NRAS
PTPN11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN11
(0.7)
ERBB3



Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Lethal congenital contracture syndrome type 2
ERBB3



Juvenile myelomonocytic leukemia
Lethal congenital contracture syndrome type 2

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

Synonym(s):
- LCCS2
- Multiple contracture syndrome, Israeli-Bedouin type

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

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

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

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

No signs/symptoms info available.