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

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

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


Citations in the biomedical literature:


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



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

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