FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term amyotrophic lateral sclerosis type 9 ID (Ontology) DOID:0060200 (Human Disease)
Definition An amyotrophic lateral sclerosis that has_material_basis_in mutation in the ANG gene on chromosome 14.
Also Known As "ALS9" ; "amyotrophic lateral sclerosis 9"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 amyotrophic lateral sclerosis type 9       1      1
 model of | amyotrophic lateral sclerosis type 9       1       --
Spanning Tree (Parents/Children)
Only view relationship: 
  motor neuron disease
   |__amyotrophic lateral sclerosis
       |__amyotrophic lateral sclerosis type 9  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a amyotrophic lateral sclerosis
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "ALS9" EXACT OMO:0003012
    "amyotrophic lateral sclerosis 9" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:10498
MIM:611895