UMLS:C0002736 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0002736 (amyotrophic lateral sclerosis)
19,048 document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
KIAA1600	10.7
KBTBD3	10.7
neurofilament-3	10.7
peroxisomal biogenesis factor 3	10.7
UBQLN2 protein	10.7
RNASE4 protein	10.7
CELF5	10.7
killer cell immunoglobulin-like receptor KIR3DL2	10.7
SYNGR4	10.7
zinc finger with KRAB and SCAN domains 3	10.7
CXX1B	10.7
RAVER1	10.7
DCTN1 protein	10.7
Histone H2B type 1-K	10.7
SUNC1	10.7
Neurofilament-light	10.7
NT5C3L	10.7
GRIA4 protein	10.7
KIAA0693	10.7
ALS	10.7
Superoxide dismutase [Cu-Zn]	10.7
Praja 1	10.7
FAM21C	10.7
ALS2CR1	10.7
CXorf64	10.7
glycosyltransferase 8 domain containing 1	10.7
KIAA1147	10.7
Smith-Magenis syndrome chromosome region, candidate 8	10.7
ANXA11 protein	10.7
Histone H2A type 1	10.7
ZNF512B	10.5
TARDBP	10.5
WDR41	10.5
FALS	10.4
FLJ10986	10.4
UBQLN2	10.4
ALS2 protein	10.4
SMCR8	10.4
C9orf72	10.4
chromosome 9 open reading frame 72	10.3

Disease
Genetic Brain Disorders	10.7
Other mental retardation	10.7
Kubisagari	10.7
Spinal cord degeneration	10.7
amyotrophic lateral sclerosis	10.7
hereditary motor and sensory neuropathy II	10.7
HMSNO	10.7
Familial motor neuron disease	10.7
ALS8	10.5
ALS6	10.5
ALS7	10.5
ALS4	10.3
FTD-ALS	10.2
ALS2	10.2
primary lateral sclerosis	10.1
Supranuclear ophthalmoplegia	10.1
ALS5	10.0
FALS	10.0
progressive bulbar palsy	9.9
Frontal lobe degeneration	9.7
CMT2A2	9.7
FTLD	9.7
progressive muscular atrophy	9.6
FUS	9.5
PLSJ	9.4
motor neuron disease	9.4
NEK1	9.2
Amyotrophic lateral sclerosis with dementia	9.1
Non-fluent aphasia	9.1
Upper motor neuron disease	9.1
Fazio-Londe	8.8
HMN7B	8.7
protein metabolism disorder	8.7
HMN V	8.7
Hereditary canine spinal muscular atrophy	8.7
IBMPFD	8.5
Dysprosody	8.4
PIN-1	8.4
SCAR8	8.4
moria	8.1

Symptom
Upper motor neuron signs	9.1
Flail	9.1
Diffuse inflammation	8.7
Glossopharyngeal breathing	8.7
amimia	8.4
Generalized fatigue	8.1
Upper back pain	8.1
fasciculation	7.4
Truncal ataxia	7.4
Muscle fibrosis	7.4
Retropulsion	7.0
disturbed speech	6.7
Limb weakness	6.5
Diaphragmatic weakness	6.5
dyslalia	6.2
dysarthria	6.2
Pyramidal signs	6.1
RNA marker	6.1
Cramping	6.1
muscle cramps	5.8
Bell's phenomenon	5.7
drooling	5.7
Spastic paraparesis	5.7
aprosodia	5.3
motor symptom	5.3
spasticity	5.2
weakness	5.2
orthopnea	5.2
arm weakness	5.2
aphagia	5.1
personality change	5.0
Severe diarrhea	4.9
Fatigability	4.7
Excitability	4.7
Urge incontinence	4.7
skin pain	4.5
asthenia	4.4
Motor dysfunction	4.3
paraparesis	4.3
ataxia	4.3

Enzyme
acetolactate synthase	6.1
MGAT	6.0
serine racemase	6.0
CCS	5.7
acetolactate decarboxylase	5.6
Alternating	5.6
galactosylhydroxylysyl glucosyltransferase	5.3
tubulin carboxypeptidase	5.3
cholesterol 25-hydroxylase	5.2
VOR	5.2
superoxide dismutase	5.2
arginyltransferase	5.1
phosphoinositide 5-phosphatase	4.8
3-mercaptopyruvate sulfurtransferase	4.8
superoxide reductase	4.8
IKK	4.5
choline dehydrogenase	4.4
E-2	4.4
CCS1	4.4
ubiquitin-protein ligase	4.2
Thy1	4.2
choline acetyltransferase	4.1
proteasome	4.1
ketohexokinase	4.0
2A protease	3.9
branched-chain aminotransferase	3.9
methionine sulfoxide reductase	3.8
caspase-4	3.8
sulfhydryl oxidase	3.8
sulfiredoxin	3.7
riboflavin kinase	3.7
caspase-4	3.6
guanidinoacetate methyltransferase	3.6
aldehyde oxidase	3.5
glycinamide ribonucleotide transformylase	3.5
cathepsin X	3.5
arachidonate 5-lipoxygenase	3.5
FADS	3.5
LIS	3.5
calpain 3	3.4