Combined immunodeficiency due to STK4 deficiency |
Frontotemporal dementia with motor neuron disease |
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INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
STK4
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Citations in the biomedical literature:
Combined immunodeficiency due to STK4 deficiency |
Frontotemporal dementia with motor neuron disease |
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Synonym(s): - CID due to STK4 deficiency
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Synonym(s): - FTD-ALS - FTD-MND - Frontotemporal dementia with amyotrophic lateral sclerosis
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Classification (Orphanet): - Rare genetic disease - Rare immune disease
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Classification (Orphanet): - Rare genetic disease - Rare neurologic disease
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Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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Classification (ICD10): (no data available)
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Epidemiological data: Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
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Epidemiological data: Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant
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External references: 1 OMIM reference -
No MeSH references | |
External references: 3 OMIM references - No MeSH references
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No signs/symptoms info available.