Preferred Name |
Amyotrophic Lateral Sclerosis |
|
Synonyms |
ALS Amyotrophic Lateral Sclerosis |
|
Definitions |
A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) |
|
ID |
http://purl.bioontology.org/ontology/MESH/D000690 |
|
altLabel |
ALS Amyotrophic Lateral Sclerosis Lou-Gehrigs Disease Disease, Guam Lou Gehrig's Disease Lou Gehrig Disease Amyotrophic Lateral Sclerosis With Dementia Gehrig Disease Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam Guam Form of Amyotrophic Lateral Sclerosis Disease, Lou-Gehrigs Motor Neuron Disease, Amyotrophic Lateral Sclerosis ALS - Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1 Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam Gehrig's Disease Gehrigs Disease Amyotrophic Lateral Sclerosis, Guam Form Charcot Disease Dementia With Amyotrophic Lateral Sclerosis Sclerosis, Amyotrophic Lateral Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1 Guam Disease |
|
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
cui |
C0002736 C0393554 C0543859 |
|
DC |
1 |
|
definition |
A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) |
|
DX |
19660101 |
|
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
Mapped from |
http://purl.bioontology.org/ontology/MESH/C564688 http://purl.bioontology.org/ontology/MESH/C566288 http://purl.bioontology.org/ontology/MESH/C563895 http://purl.bioontology.org/ontology/MESH/C564300 http://purl.bioontology.org/ontology/MESH/C567699 http://purl.bioontology.org/ontology/MESH/C566290 http://purl.bioontology.org/ontology/MESH/C531617 http://purl.bioontology.org/ontology/MESH/C538251 http://purl.bioontology.org/ontology/MESH/C567429 http://purl.bioontology.org/ontology/MESH/C567244 http://purl.bioontology.org/ontology/MESH/C565955 http://purl.bioontology.org/ontology/MESH/C565956 http://purl.bioontology.org/ontology/MESH/C565957 http://purl.bioontology.org/ontology/MESH/C566550 |
|
MDA |
19990101 |
|
MMR |
20190429 |
|
MN |
C18.452.845.800.050 C10.668.467.250 C10.574.562.250 C10.574.950.050 C10.228.854.139 |
|
notation |
D000690 |
|
prefLabel |
Amyotrophic Lateral Sclerosis |
|
TERMUI |
T366066 T814256 T840894 T366063 T002090 T366064 T000953133 T366069 T782950 T366067 T845605 T002092 T002091 T753625 T366068 |
|
TH |
BIOETHICS (1998) NLM (2000) NLM (1966) NLM (2020) NLM (1990) NLM (2012) NLM (2013) NLM (2010) GHR (2014) NLM (2014) ORD (2010) |
|
tui |
T047 |
|
subClassOf |
http://purl.bioontology.org/ontology/MESH/D057177 |