UMLS:C0476273 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0476273 (respiratory distress)
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Human Gene/Protein
latent transforming growth factor-beta binding protein 4	10.7
TRBV12-4	10.7
IGHMBP2	10.0
chromosome 9 open reading frame 116	9.7
TRBV15	9.7
KIAA0317	9.7
FAP68	9.7
ATP-binding cassette sub-family A member 3	9.4
RNFT2	9.1
TRBV30	9.1
PN-II	8.9
Transient receptor potential cation channel, subfamily V, member 6	8.7
dynein axonemal intermediate chain	8.5
Surfactant protein B	8.5
CNRG	8.3
activator of basal transcription 1	8.3
ABT1	8.3
purine-rich element binding protein A	8.3
N-heparan sulfate sulfotransferase	8.3
CCDC151	8.3
MEGF10	8.3
ABCA3	8.2
Midline-1	8.1
HOXA5 protein	8.1
SP-B	8.0
SP-C	7.9
HECTD2	7.9
RAPGEF6	7.9
pulmonary surfactant apoprotein	7.9
TMC3	7.9
EVC1	7.9
ASCC1	7.9
MBIP	7.9
MGA protein	7.9
RDS	7.8
SPAG17	7.8
SFTA3	7.7
CALR protein	7.7
SP-A1	7.5
RSPH1	7.5

Disease
lacrimal disorder	10.7
Acute subendocardial infarction	10.7
Atypical interstitial pneumonia	10.7
Lycoperdonosis	10.7
Haemophilus sepsis	10.7
Iatrogenic hypothyroidism	10.7
syndrome; 49	10.7
diffuse adenocarcinoma of the stomach	10.7
larynx; thickening	10.7
Single organ dysfunction	10.7
Congenital central alveolar hypoventilation syndrome	10.7
Chronic pulmonary insufficiency of prematurity	10.7
Laryngeal cyst	10.7
SMARD1	10.6
Neonatal respiratory distress	10.3
meconium aspiration pneumonia	10.2
Congenital pulmonary lymphangiectasis	10.0
Quail bronchitis	9.7
Interstitial pulmonary emphysema	9.7
Subglottis	9.7
Anaphylactoid syndrome of pregnancy	9.7
Pulmonary bulla	9.7
Pulmonary pneumatocele	9.7
Mixed malaria	9.7
Complete atelectasis	9.7
Multiple lung abscesses	9.7
Brooks syndrome	9.7
Acute silicosis	9.7
Transient tachypnea of newborn	9.4
Obstructive emphysema	9.3
Hemorrhagic pleural effusion	9.3
Acute respiratory distress	9.3
Neonatal listeriosis	9.2
Hyper-beta-alaninemia	9.1
Primary pulmonary hypoplasia	9.1
Nocardia sepsis	9.1
Group B streptococcal pneumonia	9.1
Acute cor pulmonale	9.1
Vallecula	9.1
Pulmonary immaturity	9.1

Symptom
Drug-induced pruritus	10.7
respiratory distress	10.7
Trepopnea	8.7
Expiratory wheezing	8.7
Diaphragmatic flutter	8.7
Polypnea	8.7
Opisthotonus	8.0
Monoparesis	7.9
Respiratory abnormalities	7.9
Inspiratory stridor	7.9
stridor	7.7
Fetal tachycardia	7.7
Central cyanosis	7.7
respiratory problem	7.6
tachypnea	7.5
Chills and fever	7.3
chest restriction	7.3
Respiratory dyskinesia	7.3
Apneusis	7.2
Acute edema	7.1
abnormal breath sounds	7.1
cyanosis	7.0
Massive edema	6.8
musculoskeletal chest pain	6.7
S3 gallop	6.6
Very Low Birth Weight	6.6
benign congenital hypotonia	6.5
Flaccid paralysis	6.5
Air trapping	6.4
Organ failure	6.3
prostration	6.2
rales	6.1
dyslalia	6.1
muscular incoordination	6.1
Diarrhea and vomiting	6.1
Poor weight gain	6.0
change in skin color	6.0
feeling sick	5.8
labored breathing	5.8
Acute dyspnea	5.7

Enzyme
phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase	8.1
angiotensin-converting enzyme 2	6.5
lysophosphatidylcholine acyltransferase	5.0
BAL	4.6
neutrophil elastase	4.5
3-hydroxy-3-methylglutaryl-CoA lyase	4.4
isovaleryl-CoA dehydrogenase	4.1
CDH	4.1
nicotinamide phosphoribosyltransferase	3.7
methylmalonyl-CoA mutase	3.6
choline kinase	3.5
ATP diphosphohydrolase	3.4
MIP	3.2
neutrophil collagenase	3.1
biotinidase	3.0
PIP kinase	3.0
elastase	2.9
ancrod	2.9
oxytocinase	2.8
E-2	2.8
sphingomyelin synthase	2.8
PPH	2.7
HVS	2.7
SOR	2.7
ADP-ribosyltransferase	2.7
Hageman factor	2.7
AGT	2.7
APC	2.6
ADP-ribosyltransferase	2.6
biliverdin reductase	2.5
ricin	2.5
prolyl hydroxylase	2.4
ACE	2.3
neutral sphingomyelinase	2.3
type III procollagen	2.2
tissue plasminogen activator	2.2
peptidylarginine deiminase	2.2
phospholipase A2	2.1
isoamylase	2.1
soluble epoxide hydrolase	2.1