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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
3 signs/symptoms
Juvenile myelomonocytic leukemia
Mucocutaneous venous malformations

CBL TEK
KRAS
NF1
NRAS
PTPN11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN11
CBL
(0.67)
(0.63)
TEK
TEK



Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Mucocutaneous venous malformations
TEK



Juvenile myelomonocytic leukemia
Mucocutaneous venous malformations

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

Synonym(s):
- Cutaneous and mucosal venous malformation
- VMCM

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare circulatory system disease
- 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:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

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

Mucocutaneous venous malformations

Very frequent
- Arteriovenous malformations / vascular malformations (excluding port-wine stains)
- Autosomal dominant inheritance
- Vascular anomalies of skin / mucosae



Juvenile myelomonocytic leukemia

(no data available)