Cytoscape Web
Click node...

Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Juvenile myelomonocytic leukemia
1 OMIM reference -
5 associated genes
No signs/symptoms info
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Juvenile myelomonocytic leukemia

TYK2
(UniProt - OMIM)
 CBL
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NF1
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PTPN11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TYK2
(0.74)
CBL


Citations in the biomedical literature:


Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
TYK2
Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11



Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Juvenile myelomonocytic leukemia

Synonym(s):
- AR hyper-IgE syndrome due to TYK2 deficiency
- AR-HIES due to TYK2 deficiency
Synonym(s):
- Juvenile chronic myelomonocytic leukemia
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D054429
No signs/symptoms info available.