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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Combined immunodeficiency due to STK4 deficiency
Progeria-associated arthropathy

STK4 LMNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
STK4
(0.63)
LMNA



Citations in the biomedical literature:


Combined immunodeficiency due to STK4 deficiency
STK4
Progeria-associated arthropathy
LMNA



Combined immunodeficiency due to STK4 deficiency
Progeria-associated arthropathy

Synonym(s):
- CID due to STK4 deficiency

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease

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