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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Unclassified chronic myeloproliferative disease

TYK2 PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TYK2
(0.65)
PDGFRB



Citations in the biomedical literature:


Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
TYK2
Unclassified chronic myeloproliferative disease
PDGFRB



Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Unclassified chronic myeloproliferative disease

Synonym(s):
- AR hyper-IgE syndrome due to TYK2 deficiency
- AR-HIES due to TYK2 deficiency

Synonym(s):
- CMPD-U
- Undifferentiated myeloproliferative disease

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:
No OMIM references
No MeSH references

No signs/symptoms info available.