Experimental Factor Ontology

Last uploaded: April 15, 2024
Preferred Name

motor neuron disease

Synonyms

ANTERIOR HORN CELL DIS

Neuron Diseases, Motor

SECOND MOTOR NEURON DIS

MOTOR NEURON DIS LOWER

UPPER MOTOR NEURON DIS

Anterior Horn Cell Disease

LOWER MOTOR NEURON DIS

MOTOR NEURON DIS UPPER

Scleroses, Lateral

Familial Motor Neuron Disease

Lateral Scleroses

FAMILIAL MOTOR NEURON DIS

Sclerosis, Lateral

Motor Neuron Disease, Lower

MOTOR NEURON DIS SECOND

Motor Neuron Disease, Upper

Motor Neuron Disease, Secondary

MOTOR SYSTEM DIS

Motor Neuron Diseases

Neuron Disease, Motor

Secondary Motor Neuron Disease

Upper Motor Neuron Disease

Lower Motor Neuron Disease

MOTOR NEURON DIS FAMILIAL

Lateral Sclerosis

MOTOR NEURON DIS

Motor Neuron Disease, Familial

Motor System Disease

Motor System Diseases

Scleroses, Primary Lateral

motor neuron disease or disorder

anterior horn cell disease

disorder of motor neuron

motor neuron disease

motor neuron disorder

disease or disorder of motor neuron

disease of motor neuron

Definitions

Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089) A disease involving the motor neuron.

ID

http://www.ebi.ac.uk/efo/EFO_0003782

closeMatch

http://identifiers.org/meddra/10028003

database_cross_reference

MeSH:D016472

SNOMEDCT:37340000

MedDRA:10028002

ICD9:335.2

Orphanet:98503

MedDRA:10028003

MONDO:0020128

DOID:231

ICD9:335.8

GARD:19477

SCTID:37340000

ICD9:335.9

ICD10CM:G12.2

MESH:D016472

definition

Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)

A disease involving the motor neuron.

disease has location

http://purl.obolibrary.org/obo/CL_0000100

exactMatch

http://purl.bioontology.org/ontology/ICD10CM/G12.2

http://identifiers.org/snomedct/37340000

http://purl.obolibrary.org/obo/Orphanet_98503

http://purl.obolibrary.org/obo/DOID_231

http://identifiers.org/mesh/D016472

has_exact_synonym

ANTERIOR HORN CELL DIS

Neuron Diseases, Motor

SECOND MOTOR NEURON DIS

MOTOR NEURON DIS LOWER

UPPER MOTOR NEURON DIS

Anterior Horn Cell Disease

LOWER MOTOR NEURON DIS

MOTOR NEURON DIS UPPER

Scleroses, Lateral

Familial Motor Neuron Disease

Lateral Scleroses

FAMILIAL MOTOR NEURON DIS

Sclerosis, Lateral

Motor Neuron Disease, Lower

MOTOR NEURON DIS SECOND

Motor Neuron Disease, Upper

Motor Neuron Disease, Secondary

MOTOR SYSTEM DIS

Motor Neuron Diseases

Neuron Disease, Motor

Secondary Motor Neuron Disease

Upper Motor Neuron Disease

Lower Motor Neuron Disease

MOTOR NEURON DIS FAMILIAL

Lateral Sclerosis

MOTOR NEURON DIS

Motor Neuron Disease, Familial

Motor System Disease

Motor System Diseases

Scleroses, Primary Lateral

motor neuron disease or disorder

anterior horn cell disease

disorder of motor neuron

motor neuron disease

motor neuron disorder

disease or disorder of motor neuron

disease of motor neuron

id

EFO:0003782

in_subset

http://purl.obolibrary.org/obo/mondo#rare

http://purl.obolibrary.org/obo/mondo#orphanet_rare

http://purl.obolibrary.org/obo/mondo#gard_rare

http://purl.obolibrary.org/obo/mondo#disease_grouping

http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders

label

motor neuron disease

notation

EFO:0003782

prefLabel

motor neuron disease

term editor

Tomasz Adamusiak

subClassOf

http://www.ebi.ac.uk/efo/EFO_0000408

http://www.ebi.ac.uk/efo/EFO_1001902

http://www.ebi.ac.uk/efo/EFO_0005772

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_231 DOID LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/37340000 SNOMEDCT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C197818 NCIT LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_231 NATPRO LOOM
http://purl.bioontology.org/ontology/ICD10CM/G12.2 ICD10CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0085084 OCHV LOOM
http://purl.obolibrary.org/obo/ND_0000119 NDDO LOOM
http://purl.obolibrary.org/obo/ND_0000119 NIO LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038384 PMAPP-PMO LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFSTD LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12565 BIRNLEX LOOM
http://www.limics.org/hrdo/rdfns#pat_id_13520 HRDO LOOM
http://doe-generated-ontology.com/OntoAD#C0085084 ONTOAD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D016472 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICD10/G12.2 ICD10 LOOM
http://www.orpha.net/ORDO/Orphanet_98503 ORDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.467 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.562 RH-MESH LOOM
http://purl.obolibrary.org/obo/DOID_231 CLO LOOM
http://purl.obolibrary.org/obo/DOID_231 DTO LOOM
http://purl.obolibrary.org/obo/DOID_231 BAO LOOM
http://purl.obolibrary.org/obo/DOID_231 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_231 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_231 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_231 FNS-H LOOM
http://purl.bioontology.org/ontology/MEDDRA/10028002 MEDDRA LOOM
http://purl.bioontology.org/ontology/ICD9CM/335.2 ICD9CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#15415 OCHV LOOM
http://purl.jp/bio/4/id/200906065489984726 IOBC LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036400 OMIM LOOM
http://www.gamuts.net/entity#motor_neuron_disease GAMUTS LOOM
http://purl.obolibrary.org/obo/OMIT_0016965 OMIT LOOM
http://purl.bioontology.org/ontology/MESH/D016472 MESH LOOM
http://purl.bioontology.org/ontology/ICPC2P/N99010 ICPC2P LOOM