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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   aortic valve insufficiency
  

Disease ID 1079
Disease aortic valve insufficiency
Definition
Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root).
Synonym
ai - aortic incompetence
aortic incompetence
aortic insufficiency
aortic regurgitation
aortic regurgitation, nos
aortic valve incompetence
aortic valve incompetence, nos
aortic valve insufficiency [disease/finding]
aortic valve insufficiency, nos
aortic valve regurgitation
aortic valve regurgitation (disorder)
aortic valve regurgitation, nos
aortic valve, incompetence
aortic valve, insufficiency
aortic valve, regurgitation
ar
ar - aortic regurgitation
incompetence, aortic
incompetence, aortic valve
insufficiency, aortic valve
regurgitation, aortic
regurgitation, aortic valve
OMIM
DOID
UMLS
C0003504
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:48)
C0003486  |  aortic aneurysm  |  13
C0003507  |  aortic stenosis  |  9
C0018801  |  heart failure  |  9
C0014118  |  endocarditis  |  6
C0020538  |  hypertension  |  6
C0018818  |  ventricular septal defect  |  4
C0020538  |  systemic hypertension  |  4
C0004943  |  behcet's disease  |  4
C0018799  |  heart disease  |  3
C0003509  |  aortitis  |  3
C0035439  |  rheumatic heart disease  |  3
C0039263  |  takayasu's arteritis  |  2
C0020443  |  hypercholesterolemia  |  2
C0409974  |  lupus erythematosus  |  2
C0014121  |  infective endocarditis  |  2
C0026266  |  mitral regurgitation  |  2
C0040961  |  tricuspid regurgitation  |  2
C0024141  |  systemic lupus erythematosus  |  2
C0034063  |  pulmonary edema  |  1
C0003511  |  syphilitic aortitis  |  1
C0020542  |  pulmonary hypertension  |  1
C0003486  |  aortic aneurysms  |  1
C0004153  |  atherosclerosis  |  1
C0020445  |  familial hypercholesterolemia  |  1
C0153500  |  heart ca  |  1
C0085435  |  reactive arthritis  |  1
C0002871  |  anemia  |  1
C0002878  |  hemolytic anemia  |  1
C0027051  |  myocardial infarct  |  1
C0152101  |  hypoplastic left heart syndrome  |  1
C0020443  |  hypercholesterolaemia  |  1
C0022116  |  ischemia  |  1
C0162872  |  thoracic aortic aneurysm  |  1
C0031036  |  polyarteritis nodosa  |  1
C0018802  |  congestive cardiac failure  |  1
C0018801  |  cardiac failure  |  1
C0027051  |  myocardial infarction  |  1
C0010051  |  coronary aneurysms  |  1
C0040053  |  thrombus  |  1
C0018802  |  congestive heart failure  |  1
C0010051  |  coronary aneurysm  |  1
C0012628  |  discrete subaortic stenosis  |  1
C0029434  |  osteogenesis imperfecta  |  1
C0003505  |  aortic valve prolapse  |  1
C0039263  |  takayasu disease  |  1
C0039263  |  takayasu arteritis  |  1
C0152101  |  hypoplastic left heart  |  1
C0155733  |  aortic atherosclerosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:12)
4878  |  NPPA  |  CTD_human
7040  |  TGFB1  |  CTD_human
1277  |  COL1A1  |  CTD_human
2335  |  FN1  |  CTD_human
11167  |  FSTL1  |  CTD_human
4879  |  NPPB  |  CTD_human
1490  |  CTGF  |  CTD_human
7076  |  TIMP1  |  CTD_human
7042  |  TGFB2  |  CTD_human
1281  |  COL3A1  |  CTD_human
4015  |  LOX  |  CTD_human
231  |  AKR1B1  |  OMIM
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:79)
55256  |  ADI1  |  2.586  |  DISEASES
84890  |  ADO  |  2  |  DISEASES
183  |  AGT  |  1.019  |  DISEASES
186  |  AGTR2  |  1.442  |  DISEASES
64400  |  AKTIP  |  1.09  |  DISEASES
10189  |  ALYREF  |  2.771  |  DISEASES
25820  |  ARIH1  |  3.138  |  DISEASES
415  |  ARSE  |  1.242  |  DISEASES
10159  |  ATP6AP2  |  1.127  |  DISEASES
554  |  AVPR2  |  1.344  |  DISEASES
7917  |  BAG6  |  1.331  |  DISEASES
650  |  BMP2  |  1.117  |  DISEASES
78996  |  C7orf49  |  2.331  |  DISEASES
1025  |  CDK9  |  1.58  |  DISEASES
9350  |  CER1  |  1.714  |  DISEASES
27297  |  CRCP  |  2.081  |  DISEASES
78987  |  CRELD1  |  1.031  |  DISEASES
9547  |  CXCL14  |  2.072  |  DISEASES
91319  |  DERL3  |  2.61  |  DISEASES
6993  |  DYNLT1  |  1.4  |  DISEASES
10969  |  EBNA1BP2  |  2.96  |  DISEASES
10919  |  EHMT2  |  1.251  |  DISEASES
2155  |  F7  |  1.433  |  DISEASES
2192  |  FBLN1  |  1.587  |  DISEASES
10516  |  FBLN5  |  1.412  |  DISEASES
2200  |  FBN1  |  3.347  |  DISEASES
2316  |  FLNA  |  1.168  |  DISEASES
4303  |  FOXO4  |  1.944  |  DISEASES
2524  |  FUT2  |  3.364  |  DISEASES
54826  |  GIN1  |  2.241  |  DISEASES
3055  |  HCK  |  2.591  |  DISEASES
3106  |  HLA-B  |  1.912  |  DISEASES
3112  |  HLA-DOB  |  1.629  |  DISEASES
3240  |  HP  |  1.269  |  DISEASES
133396  |  IL31RA  |  1.007  |  DISEASES
259307  |  IL4I1  |  4.092  |  DISEASES
57611  |  ISLR2  |  2.456  |  DISEASES
3725  |  JUN  |  1.285  |  DISEASES
102723508  |  KANTR  |  1.297  |  DISEASES
154881  |  KCTD7  |  2.053  |  DISEASES
9851  |  KIAA0753  |  1.742  |  DISEASES
1316  |  KLF6  |  1.153  |  DISEASES
26524  |  LATS2  |  1.222  |  DISEASES
54900  |  LAX1  |  1.857  |  DISEASES
440900  |  LINC01191  |  3.234  |  DISEASES
10747  |  MASP2  |  1.494  |  DISEASES
83881  |  MIXL1  |  1.413  |  DISEASES
344022  |  NOTO  |  1.904  |  DISEASES
4878  |  NPPA  |  2.399  |  DISEASES
4879  |  NPPB  |  3.152  |  DISEASES
4882  |  NPR2  |  1.869  |  DISEASES
7182  |  NR2C2  |  2.299  |  DISEASES
390874  |  ONECUT3  |  1.995  |  DISEASES
10015  |  PDCD6IP  |  2.477  |  DISEASES
54704  |  PDP1  |  2.024  |  DISEASES
8544  |  PIR  |  1.288  |  DISEASES
5309  |  PITX3  |  1.254  |  DISEASES
5329  |  PLAUR  |  2.121  |  DISEASES
57449  |  PLEKHG5  |  3.032  |  DISEASES
5538  |  PPT1  |  1.08  |  DISEASES
145270  |  PRIMA1  |  2.392  |  DISEASES
5799  |  PTPRN2  |  3.069  |  DISEASES
5900  |  RALGDS  |  3.506  |  DISEASES
9939  |  RBM8A  |  1.821  |  DISEASES
80196  |  RNF34  |  1.998  |  DISEASES
6227  |  RPS21  |  2.345  |  DISEASES
55511  |  SAGE1  |  1.975  |  DISEASES
404552  |  SCGB1D4  |  1.253  |  DISEASES
140885  |  SIRPA  |  2.087  |  DISEASES
388588  |  SMIM1  |  1.827  |  DISEASES
23583  |  SMUG1  |  1.307  |  DISEASES
6714  |  SRC  |  2.245  |  DISEASES
117178  |  SSX2IP  |  4.06  |  DISEASES
6942  |  TCF20  |  1.757  |  DISEASES
7137  |  TNNI3  |  1.473  |  DISEASES
7706  |  TRIM25  |  2.548  |  DISEASES
51366  |  UBR5  |  2.172  |  DISEASES
7409  |  VAV1  |  1.026  |  DISEASES
9278  |  ZBTB22  |  1.28  |  DISEASES
Locus(Waiting for update.)
Disease ID 1079
Disease aortic valve insufficiency
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:50)
HP:0002617  |  Aneurysmal dilatation  |  29
HP:0004942  |  Aortic aneurysm  |  13
HP:0001635  |  Congestive heart failure  |  10
HP:0001650  |  Valvular aortic stenosis  |  10
HP:0001647  |  Bicuspid aortic valve  |  9
HP:0002616  |  Aortic root dilatation  |  8
HP:0002631  |  Ascending aortic aneurysm  |  8
HP:0011645  |  Aneurysm of the aortic sinus  |  7
HP:0000822  |  Hypertension  |  7
HP:0100584  |  Endocarditis  |  5
HP:0001714  |  Ventricular hypertrophy  |  4
HP:0001712  |  Left ventricular hypertrophy  |  4
HP:0001629  |  Ventricular septal defects  |  4
HP:0002647  |  Aortic dissection  |  4
HP:0012089  |  Arteritis  |  3
HP:0003124  |  Elevated serum cholesterol  |  2
HP:0001724  |  Aortic dilatation  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0000969  |  Dropsy  |  2
HP:0006689  |  Bacterial endocarditis  |  2
HP:0005111  |  Dilation of the ascending aorta  |  2
HP:0005180  |  Tricuspid insufficiency  |  2
HP:0001260  |  Dysarthric speech  |  2
HP:0001653  |  Mitral valve insufficiency  |  2
HP:0002621  |  Atherosclerosis  |  1
HP:0004380  |  Aortic valve calcification  |  1
HP:0012727  |  Thoracic aortic aneurysm  |  1
HP:0012382  |  Left-to-right shunt  |  1
HP:0002094  |  Dyspnea  |  1
HP:0001662  |  Bradycardia  |  1
HP:0030149  |  Cardiovascular shock  |  1
HP:0001634  |  Mitral valve prolapse  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0006698  |  Ventricular aneurysm  |  1
HP:0002092  |  Pulmonary artery hypertension  |  1
HP:0100598  |  Pulmonary oedema  |  1
HP:0005110  |  Atrial fibrillation  |  1
HP:0012561  |  Unicuspid aortic valve  |  1
HP:0001682  |  Subvalvular aortic stenosis  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0001669  |  Transposition of the great arteries  |  1
HP:0012764  |  Orthopnea  |  1
HP:0004383  |  Underdeveloped left heart  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0001903  |  Anemia  |  1
HP:0001680  |  Coarctation of aorta  |  1
HP:0004947  |  Arteriovenous fistula  |  1
HP:0012397  |  Atherosclerotic changes of aorta  |  1
HP:0012418  |  Low blood oxygen level  |  1
HP:0001658  |  Myocardial infarction  |  1
Disease ID 1079
Disease aortic valve insufficiency
Manually Symptom
UMLS  | Name(Total Manually Symptoms:7)
C0920035  |  left ventricular overload
C0027051  |  myocardial infarct
C0018818  |  ventricular septal defects
C0003510  |  aortitis syndrome
C0003509  |  aortitis
C0003486  |  aortic aneurysms
C0002940  |  aneurysm
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:14)
C0002940  |  aneurysm  |  19
C0018801  |  heart failure  |  8
C0003486  |  aortic aneurysm  |  5
C0018818  |  ventricular septal defect  |  4
C0232262  |  diastolic murmur  |  3
C0340643  |  aortic dissection  |  3
C0856747  |  ascending aortic aneurysm  |  3
C0020538  |  hypertension  |  1
C0519097  |  left ventricular aneurysm  |  1
C0018802  |  congestive heart failure  |  1
C0018801  |  cardiac failure  |  1
C0003486  |  aortic aneurysms  |  1
C0013404  |  dyspnea  |  1
C0020542  |  pulmonary hypertension  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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.)
Disease ID 1079
Disease aortic valve insufficiency
Case(Waiting for update.)