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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
amyotrophic lateral sclerosis type 1  
amyotrophic lateral sclerosis type 10  
amyotrophic lateral sclerosis type 11  
amyotrophic lateral sclerosis type 12  
amyotrophic lateral sclerosis type 13 
amyotrophic lateral sclerosis type 15  
amyotrophic lateral sclerosis type 16  
amyotrophic lateral sclerosis type 18  
amyotrophic lateral sclerosis type 19  
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the ERBB4 gene on chromosome 2. (DO)
amyotrophic lateral sclerosis type 20  
amyotrophic lateral sclerosis type 21  
amyotrophic lateral sclerosis type 22  
amyotrophic lateral sclerosis type 23  
amyotrophic lateral sclerosis type 24  
amyotrophic lateral sclerosis type 25  
amyotrophic lateral sclerosis type 26  
amyotrophic lateral sclerosis type 28  
amyotrophic lateral sclerosis type 3 
amyotrophic lateral sclerosis type 6  
amyotrophic lateral sclerosis type 7 
amyotrophic lateral sclerosis type 8  
amyotrophic lateral sclerosis type 9  
Amyotrophic Lateral Sclerosis with Polyglucosan Bodies 
Amyotrophic Lateral Sclerosis, Autosomal Recessive  
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1  
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis +   
Juvenile Amyotrophic Lateral Sclerosis +   
sporatic amyotrophic lateral sclerosis 

Synonyms
Exact Synonyms: ALS19 ;   ERBB4-RELATED CONDITION ;   amyotrophic lateral sclerosis 19
Primary IDs: OMIM:615515
Alternate IDs: RDO:9000975
Definition Sources: http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis "DO" "DO", http://omim.org/entry/615515 "DO" "DO"

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