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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Chronic myelomonocytic leukemia
Laron syndrome with immunodeficiency

ETV6 STAT5B
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
(0.52)
STAT5B



Citations in the biomedical literature:


Chronic myelomonocytic leukemia
ETV6 PDGFRB
Laron syndrome with immunodeficiency
STAT5B



Chronic myelomonocytic leukemia
Laron syndrome with immunodeficiency

Synonym(s):
(no synonyms)

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

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
1 MeSH reference: D015477
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.