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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 10
20 associated genes
No signs/symptoms info
Hypohidrotic ectodermal dysplasia with immunodeficiency
Precursor T-cell acute lymphoblastic leukemia

IKBKG ABL1
NFKBIA BCR
CDKN2A
CNOT3
DDX3X
FLT3
HNRNPH1
MLLT10
MYB
MYC
PICALM
STIL
TAL1
TCL1A
TLX1
TLX3
TRA
()
TRB
TRD
TRG
()


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
IKBKG
IKBKG
IKBKG
NFKBIA
IKBKG
IKBKG
IKBKG
NFKBIA
NFKBIA
NFKBIA
(0.75)
(0.73)
(0.68)
(0.68)
(0.63)
(0.63)
(0.63)
(0.63)
(0.63)
(0.63)
DDX3X
MYC
FLT3
ABL1
TRA
TRD
TRG
TRA
TRD
TRG



Citations in the biomedical literature:


Hypohidrotic ectodermal dysplasia with immunodeficiency
IKBKG NFKBIA
Precursor T-cell acute lymphoblastic leukemia
ABL1 BCR CDKN2A CNOT3 DDX3X FLT3
HNRNPH1 MLLT10 MYB MYC PICALM STIL
TAL1 TCL1A TLX1 TLX3 TRA TRB
TRD TRG



Hypohidrotic ectodermal dysplasia with immunodeficiency
Precursor T-cell acute lymphoblastic leukemia

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

Synonym(s):
- Precursor T-cell acute lymphoblastic leukemia/lymphoma
- Precursor T-cell acute lymphocytic leukemia
- Precursor T-cell acute lymphocytic leukemia/lymphoma
- T-ALL

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:
(no data available)

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

No signs/symptoms info available.