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Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Combined immunodeficiency due to STK4 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Combined immunodeficiency due to STK4 deficiency

RPS14
(UniProt - OMIM)
 STK4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RPS14
(0.63)
STK4


Citations in the biomedical literature:


Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
RPS14
Combined immunodeficiency due to STK4 deficiency
STK4



Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Combined immunodeficiency due to STK4 deficiency

Synonym(s):
- 5q- syndrome
Synonym(s):
- CID due to STK4 deficiency
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- 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: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.