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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Laron syndrome with immunodeficiency
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

STAT5B CREBBP
KAT6A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
STAT5B
(0.63)
CREBBP



Citations in the biomedical literature:


Laron syndrome with immunodeficiency
STAT5B
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
CREBBP KAT6A



Laron syndrome with immunodeficiency
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

Synonym(s):
- Laron-like syndrome
- Short stature due to STAT5b deficiency

Synonym(s):
(no synonyms)

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: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal 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.