Cytoscape Web
Click node...


2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 5
6 OMIM references -
7 associated genes
No signs/symptoms info
Hypohidrotic ectodermal dysplasia with immunodeficiency
B-cell chronic lymphocytic leukemia

IKBKG ARL11
NFKBIA ATM
CCND1
IGHG1
IGHV3-21
()
POT1
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NFKBIA
IKBKG
IKBKG
IKBKG
NFKBIA
(0.94)
(0.85)
(0.72)
(0.63)
(0.63)
TP53
ATM
IGHG1
IGHV3-21
IGHV3-21



Citations in the biomedical literature:


Hypohidrotic ectodermal dysplasia with immunodeficiency
IKBKG NFKBIA
B-cell chronic lymphocytic leukemia
ARL11 ATM CCND1 IGHG1 IGHV3-21 POT1
TP53



Hypohidrotic ectodermal dysplasia with immunodeficiency
B-cell chronic lymphocytic leukemia

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

Synonym(s):
- B-CLL
- B-cell chronic lymphoid leukemia
- Lymphoplasmacytic leukemia
- Lymphoplasmacytoid immunocytoma
- Small lymphocytic lymphoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
- Rare skin 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:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
2 OMIM references -
No MeSH references
External references:
6 OMIM references -
1 MeSH reference: D015451

No signs/symptoms info available.