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DO Term : amyotrophic lateral sclerosis [DOID:332] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.

synonyms:
ORDO:803,
SNOMEDCT_US_2023_03_01:86044005,
ICD10CM:G12.21,
UMLS_CUI:C0002736,
motor neuron disease, bulbar,
MESH:D000690,
ALS,
GARD:5786,
NCI:C34373,
Lou Gehrig's disease,
ICD9CM:335.20,
OMIM:PS105400,
PS105400,
KEGG:05014

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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