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Amyotrophic lateral sclerosis type 4
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Spinocerebellar ataxia with axonal neuropathy type 2
Apolipoprotein A-I deficiency
Congenital analbuminemia
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Burkitt lymphoma
Congenital atransferrinemia
Precursor T-cell acute lymphoblastic leukemia
Synonym(s):
- ALS4
- Distal hereditary motor neuropathy with upper motor neuron signs
- dHMN with upper motor neuron signs
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SETX Q7Z333608465
No signs/symptoms info available.