PedAM

Pediatric Disease Annotations & Medicines


	myocardial stunning

Disease ID	1520
Disease	myocardial stunning
Definition	Prolonged dysfunction of the myocardium after a brief episode of severe ischemia, with gradual return of contractile activity.
Synonym	myocardial stunning [disease/finding] stunning, myocardial
DOID	DOID:9767
UMLS	C0206146
MeSH	D017682
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:9) C0027059 \| myocarditis \| 1 C0022116 \| ischaemia \| 1 C0034063 \| pulmonary edema \| 1 C0155626 \| acute myocardial infarction \| 1 C0027051 \| myocardial infarct \| 1 C0010073 \| coronary artery spasm \| 1 C0018799 \| heart disease \| 1 C0022116 \| ischemia \| 1 C0027051 \| myocardial infarction \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:4) TNF \| 7124 \| CTD_human ATP2A2 \| 488 \| CTD_human NOS2 \| 4843 \| CTD_human PLN \| 5350 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:98) 10344 \| CCL26 \| DISEASES 3162 \| HMOX1 \| DISEASES 51804 \| SIX4 \| DISEASES 7076 \| TIMP1 \| DISEASES 4313 \| MMP2 \| DISEASES 6783 \| SULT1E1 \| DISEASES 1410 \| CRYAB \| DISEASES 4633 \| MYL2 \| DISEASES 471 \| ATIC \| DISEASES 6945 \| MLX \| DISEASES 3315 \| HSPB1 \| DISEASES 7014 \| TERF2 \| DISEASES 109 \| ADCY3 \| DISEASES 3417 \| IDH1 \| DISEASES 5687 \| PSMA6 \| DISEASES 3674 \| ITGA2B \| DISEASES 5976 \| UPF1 \| DISEASES 2769 \| GNA15 \| DISEASES 6403 \| SELP \| DISEASES 6548 \| SLC9A1 \| DISEASES 3383 \| ICAM1 \| DISEASES 3827 \| KNG1 \| DISEASES 805 \| CALM2 \| DISEASES 10398 \| MYL9 \| DISEASES 1525 \| CXADR \| DISEASES 231 \| AKR1B1 \| DISEASES 7079 \| TIMP4 \| DISEASES 1636 \| ACE \| DISEASES 808 \| CALM3 \| DISEASES 4880 \| NPPC \| DISEASES 4846 \| NOS3 \| DISEASES 27343 \| POLL \| DISEASES 3308 \| HSPA4 \| DISEASES 8988 \| HSPB3 \| DISEASES 1448 \| CSN3 \| DISEASES 1938 \| EEF2 \| DISEASES 134 \| ADORA1 \| DISEASES 171389 \| NLRP6 \| DISEASES 358 \| AQP1 \| DISEASES 147912 \| SIX5 \| DISEASES 2744 \| GLS \| DISEASES 23019 \| CNOT1 \| DISEASES 4843 \| NOS2 \| DISEASES 5069 \| PAPPA \| DISEASES 6401 \| SELE \| DISEASES 3418 \| IDH2 \| DISEASES 168374 \| ZNF92 \| DISEASES 23583 \| SMUG1 \| DISEASES 4137 \| MAPT \| DISEASES 7137 \| TNNI3 \| DISEASES 3767 \| KCNJ11 \| DISEASES 801 \| CALM1 \| DISEASES 487 \| ATP2A1 \| DISEASES 4606 \| MYBPC2 \| DISEASES 6714 \| SRC \| DISEASES 4151 \| MB \| DISEASES 1565 \| CYP2D6 \| DISEASES 23038 \| WDTC1 \| DISEASES 7139 \| TNNT2 \| DISEASES 5743 \| PTGS2 \| DISEASES 462 \| SERPINC1 \| DISEASES 153 \| ADRB1 \| DISEASES 26227 \| PHGDH \| DISEASES 140 \| ADORA3 \| DISEASES 2030 \| SLC29A1 \| DISEASES 4318 \| MMP9 \| DISEASES 6709 \| SPTAN1 \| DISEASES 80312 \| TET1 \| DISEASES 84890 \| ADO \| DISEASES 9966 \| TNFSF15 \| DISEASES 3303 \| HSPA1A \| DISEASES 4879 \| NPPB \| DISEASES 10529 \| NEBL \| DISEASES 57380 \| MRS2 \| DISEASES 1906 \| EDN1 \| DISEASES 1107 \| CHD3 \| DISEASES 9350 \| CER1 \| DISEASES 2281 \| FKBP1B \| DISEASES 6649 \| SOD3 \| DISEASES 831 \| CAST \| DISEASES 23365 \| ARHGEF12 \| DISEASES 10410 \| IFITM3 \| DISEASES 501 \| ALDH7A1 \| DISEASES 3112 \| HLA-DOB \| DISEASES 8671 \| SLC4A4 \| DISEASES 279 \| AMY2A \| DISEASES 9498 \| SLC4A8 \| DISEASES 10189 \| ALYREF \| DISEASES 342538 \| NACA2 \| DISEASES 57451 \| TENM2 \| DISEASES 2053 \| EPHX2 \| DISEASES 4607 \| MYBPC3 \| DISEASES 5125 \| PCSK5 \| DISEASES 8972 \| MGAM \| DISEASES 5228 \| PGF \| DISEASES 3316 \| HSPB2 \| DISEASES 7138 \| TNNT1 \| DISEASES 102723508 \| KANTR \| DISEASES
Locus	(Waiting for update.)

Disease ID	1520
Disease	myocardial stunning
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:6) HP:0001250 \| Seizures \| 1 HP:0002615 \| Low blood pressure \| 1 HP:0000969 \| Dropsy \| 1 HP:0001658 \| Myocardial infarction \| 1 HP:0100598 \| Pulmonary oedema \| 1 HP:0012819 \| Myocarditis \| 1

Disease ID	1520
Disease	myocardial stunning
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0022116 \| ischemia \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Chemical(Total Drugs:2)
CUI	ChemicalName	ChemicalID	CasRN	DiseaseName	DiseaseID	DirectEvidence	PubMedIDs
C0206146	fluorouracil	D005472	51-21-8	myocardial stunning	MESH:D017682	marker/mechanism	2205312
C0206146	phenylephrine	D010656	59-42-7	myocardial stunning	MESH:D017682	marker/mechanism	7772323

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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