OBO ID: DOID:0060196
Term Name: amyotrophic lateral sclerosis type 4 Search Ontology:
Synonyms:
  • ALS 4
  • amyotrophic lateral sclerosis 4
  • amyotrophic lateral sclerosis 4, juvenile
  • dHMN with upper motor neuron signs
  • distal hereditary motor neuropathy with pyramidal features
  • distal hereditary motor neuropathy with upper motor neuron signs
Definition: An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9. (2)
References:
Ontology: Human Disease   ( DOID:0060196 )
Relationships
is a type of:
OTHER amyotrophic lateral sclerosis type 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SETX Amyotrophic lateral sclerosis 4, juvenile 602433
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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