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Autosomal recessive lymphoproliferative disease
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hypohidrotic ectodermal dysplasia with immunodeficiency
2 OMIM references -
2 associated genes
No signs/symptoms info
Autosomal recessive lymphoproliferative disease
Hypohidrotic ectodermal dysplasia with immunodeficiency

CD27
(UniProt - OMIM)
 IKBKG
(UniProt - OMIM)
ITK
(UniProt - OMIM)
 NFKBIA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ITK
(0.68)
IKBKG


Citations in the biomedical literature:


Autosomal recessive lymphoproliferative disease
CD27 ITK
Hypohidrotic ectodermal dysplasia with immunodeficiency
IKBKG NFKBIA



Autosomal recessive lymphoproliferative disease
Hypohidrotic ectodermal dysplasia with immunodeficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Anhidrotic ectodermal dysplasia with immunodeficiency
- EDA-ID
- HED-ID
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
- Rare skin disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.