Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

motor neuron disease

Synonyms

Sclerosis, Lateral

motor neuron disease

Motor System Diseases

Neuron Diseases, Motor

ANTERIOR HORN CELL DIS

Motor System Disease

Scleroses, Lateral

disease of motor neuron

MOTOR NEURON DIS SECOND

Lateral Sclerosis

MOTOR NEURON DIS LOWER

disease or disorder of motor neuron

MOTOR NEURON DIS UPPER

Secondary Motor Neuron Disease

Motor Neuron Disease, Upper

FAMILIAL MOTOR NEURON DIS

Neuron Disease, Motor

motor neuron disease or disorder

anterior horn cell disease

Upper Motor Neuron Disease

Anterior Horn Cell Disease

Lower Motor Neuron Disease

MOTOR NEURON DIS

MOTOR SYSTEM DIS

MOTOR NEURON DIS FAMILIAL

Familial Motor Neuron Disease

Scleroses, Primary Lateral

LOWER MOTOR NEURON DIS

Motor Neuron Disease, Secondary

Motor Neuron Disease, Familial

UPPER MOTOR NEURON DIS

Lateral Scleroses

SECOND MOTOR NEURON DIS

Motor Neuron Disease, Lower

disorder of motor neuron

Motor Neuron Diseases

Definitions

A disease involving the motor neuron. 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)

ID

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

closeMatch

http://identifiers.org/snomedct/192890000

http://linkedlifedata.com/resource/umls/id/C0154681

http://identifiers.org/snomedct/155015007

http://identifiers.org/snomedct/192888001

http://identifiers.org/snomedct/192889009

database_cross_reference

MSH:D016472

ICD9:335.2

ICD10:G12.20

ICD9:335.8

COHD:374631

SCTID:37340000

ICD10:G12.2

MESH:D016472

Orphanet:98503

SNOMEDCT:37340000

ICD9:335.9

MONDO:0020128

MedDRA:10028003

DOID:231

definition

A disease involving the motor neuron.

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)

exactMatch

http://identifiers.org/meddra/10028003

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

http://linkedlifedata.com/resource/umls/id/C0085084

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

http://identifiers.org/snomedct/37340000

http://identifiers.org/mesh/D016472

has_exact_synonym

Sclerosis, Lateral

motor neuron disease

Motor System Diseases

Neuron Diseases, Motor

ANTERIOR HORN CELL DIS

Motor System Disease

Scleroses, Lateral

disease of motor neuron

MOTOR NEURON DIS SECOND

Lateral Sclerosis

MOTOR NEURON DIS LOWER

disease or disorder of motor neuron

MOTOR NEURON DIS UPPER

Secondary Motor Neuron Disease

Motor Neuron Disease, Upper

FAMILIAL MOTOR NEURON DIS

Neuron Disease, Motor

motor neuron disease or disorder

anterior horn cell disease

Upper Motor Neuron Disease

Anterior Horn Cell Disease

Lower Motor Neuron Disease

MOTOR NEURON DIS

MOTOR SYSTEM DIS

MOTOR NEURON DIS FAMILIAL

Familial Motor Neuron Disease

Scleroses, Primary Lateral

LOWER MOTOR NEURON DIS

Motor Neuron Disease, Secondary

Motor Neuron Disease, Familial

UPPER MOTOR NEURON DIS

Lateral Scleroses

SECOND MOTOR NEURON DIS

Motor Neuron Disease, Lower

disorder of motor neuron

Motor Neuron Diseases

has_related_synonym

disorder of motor neuron

id

EFO:0003782

in_subset

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_0005772

http://purl.obolibrary.org/obo/MONDO_0044979

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

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http://purl.obolibrary.org/obo/ND_0000119 NDDO LOOM
http://purl.obolibrary.org/obo/ND_0000119 NDDO LOOM
http://purl.obolibrary.org/obo/DOID_231 BAO LOOM
http://purl.obolibrary.org/obo/DOID_231 DTO LOOM
http://purl.obolibrary.org/obo/DOID_231 CLO LOOM
http://purl.obolibrary.org/obo/DOID_231 BAO LOOM
http://purl.obolibrary.org/obo/DOID_231 DOID LOOM
http://purl.obolibrary.org/obo/DOID_231 NIFSTD LOOM
http://purl.bioontology.org/ontology/ICD10CM/G12.2 ICD10CM LOOM
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http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.562 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/37340000 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/ICPC2P/N99010 ICPC2P LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036400 OMIM LOOM
http://purl.bioontology.org/ontology/ICD10/G12.2 ICD10 LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFSTD LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_231 NATPRO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D016472 RH-MESH LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 MONDO SAME_URI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 EFO SAME_URI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 EFO SAME_URI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 EFO SAME_URI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 EFO SAME_URI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003782 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0020128 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0020128 MONDO LOOM
http://www.orpha.net/ORDO/Orphanet_98503 ORDO LOOM
http://www.orpha.net/ORDO/Orphanet_98503 ORDO LOOM
http://www.orpha.net/ORDO/Orphanet_98503 HORD LOOM
http://www.orpha.net/ORDO/Orphanet_98503 ORDO LOOM
http://purl.bioontology.org/ontology/ICD9CM/335.2 ICD9CM 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#C10.668.467 RH-MESH LOOM
http://purl.bioontology.org/ontology/MESH/D016472 MESH LOOM
http://purl.bioontology.org/ontology/MEDDRA/10028002 MEDDRA LOOM
http://purl.jp/bio/4/id/200906065489984726 IOBC LOOM
http://purl.jp/bio/4/id/200906065489984726 IOBC LOOM
http://purl.jp/bio/4/id/200906065489984726 IOBC LOOM