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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
6 associated genes
No signs/symptoms info
Hypohidrotic ectodermal dysplasia with immunodeficiency
Inflammatory myofibroblastic tumor

IKBKG ALK
NFKBIA CARS
CLTC
RANBP2
TPM3
TPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
IKBKG
NFKBIA
IKBKG
(0.72)
(0.63)
(0.56)
CLTC
CLTC
ALK



Citations in the biomedical literature:


Hypohidrotic ectodermal dysplasia with immunodeficiency
IKBKG NFKBIA
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Hypohidrotic ectodermal dysplasia with immunodeficiency
Inflammatory myofibroblastic tumor

Synonym(s):
- Anhidrotic ectodermal dysplasia with immunodeficiency
- EDA-ID
- HED-ID

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.