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PROTEIN INTERACTIONS: 2
5 associated genes
No signs/symptoms info
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

BTK CEBPA
ELF4 FLT3
KIT
RUNX1
RUNX1T1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ELF4
BTK
(0.89)
(0.52)
RUNX1
KIT



Citations in the biomedical literature:


Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
BTK ELF4
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 KIT RUNX1 RUNX1T1



Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare immune 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: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.