UMLS:C0014848 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0014848 (achalasia)
2,804 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Human Gene/Protein
ADRACALIN	13.5
GDP-mannose pyrophosphorylase A	13.5
achalasia variant	12.5
GMPPA	12.2
AAAS	12.2
POEM	10.7
GUCY1A3	10.1
FGD2	9.9
FGD3	9.7
GP210	9.6
GMPPB	9.4
nuclear pore protein	8.9
MRAP	8.8
TPIT	8.7
COL4A6	8.5
TXNRD2	8.3
NDC1	8.2
thioredoxin reductase 2	8.1
nuclear pore complex protein	8.1
ACTH receptor	8.0

Disease
NID A	13.5
Rectosigmoid junction	13.5
achalasia	13.5
Atypical bulimia nervosa	13.5
Rectosigmoid junction	13.5
Primary achalasia	13.1
Heller	12.6
esophageal spasm	12.5
Familial visceral neuropathy	12.5
Nutcracker esophagus	11.9
Intestinal Dysplasia	11.9
Esophageal erosions	11.9
Cricopharyngeal achalasia	11.8
Esophageal dysphagia	11.7
NID B	11.5
megaesophagus	11.4
chalasia	11.2
Inflammatory neuropathy	10.7
Schatzki's ring	10.5
CISS1	10.5

Enzyme
GDP-mannose pyrophosphorylase	7.0
botulinum neurotoxin	4.6
transhydrogenase	4.0
MCS	3.9
NADPH-diaphorase	3.9
ubiquitin-protein ligase	3.8
dihydropyrimidine dehydrogenase	3.8
dihydropyrimidine dehydrogenase	3.2
dopamine beta-hydroxylase	3.0
PRA	2.8
guanylate cyclase	2.7
prostate-specific membrane antigen	2.7
NOS	2.6
enolase	2.6
NO synthase	2.3
hypoxanthine-guanine phosphoribosyltransferase	2.2
myosin light chain kinase	2.1
protein phosphatase 2A	1.9
granzyme B	1.8
UDP-glucuronosyltransferase	1.8