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Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant centronuclear myopathy
2 OMIM references -
4 associated genes
No signs/symptoms info
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Autosomal dominant centronuclear myopathy

TYK2
(UniProt - OMIM)
 DNM2
(UniProt - OMIM)
MTMR14
(UniProt - OMIM)
MYF6
(UniProt - OMIM)
RYR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TYK2
(0.63)
DNM2


Citations in the biomedical literature:


Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
TYK2
Autosomal dominant centronuclear myopathy
DNM2 MTMR14 MYF6 RYR1



Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Autosomal dominant centronuclear myopathy

Synonym(s):
- AR hyper-IgE syndrome due to TYK2 deficiency
- AR-HIES due to TYK2 deficiency
Synonym(s):
- AD-CNM
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.