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encyclopedia of Rare Disease Annotation for Precision Medicine



   hypoplastic left heart syndrome
  

Disease ID 8
Disease hypoplastic left heart syndrome
Definition
A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (HEART ATRIUM; HEART VENTRICLE), the AORTA, the AORTIC VALVE, and the MITRAL VALVE. Severe symptoms appear in early infancy when DUCTUS ARTERIOSUS closes.
Synonym
heart hypoplastic left
heart hypoplastic left syndrome
hlh - hypoplastic left heart syndrome
hlhs
hlhs - hypoplastic left heart syndrome
hlhs1
hypoplas left heart synd
hypoplasia left heart
hypoplastic left heart
hypoplastic left heart syndrome (disorder)
hypoplastic left heart syndrome 1
hypoplastic left heart syndrome [disease/finding]
left heart hypoplasia syndrome
left heart hypoplastic
left heart syndrome, hypoplastic
left hypoplastic heart
underdeveloped left heart
Orphanet
OMIM
DOID
ICD10
UMLS
C0152101
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:15)
C0003507  |  aortic stenosis  |  10
C0040961  |  tricuspid regurgitation  |  4
C1956257  |  pulmonary stenosis  |  2
C0152021  |  congenital heart disease  |  2
C0796004  |  kabuki syndrome  |  2
C0003504  |  aortic regurgitation  |  1
C0003507  |  aortic valve stenosis  |  1
C0795690  |  omphalocele  |  1
C0018799  |  heart diseases  |  1
C0018801  |  heart failure  |  1
C0014117  |  endocardial fibroelastosis  |  1
C0028326  |  noonan syndrome  |  1
C0018799  |  heart disease  |  1
C0040961  |  tricuspid valve regurgitation  |  1
C0034089  |  pulmonary valve stenosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
1482  |  NKX2-5  |  ORPHANET
2697  |  GJA1  |  CLINVAR;CTD_human;ORPHANET;UNIPROT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
1906  |  EDN1  |  CIPHER
2697  |  GJA1  |  CIPHER;CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:46)
111  |  ADCY5  |  1.994  |  DISEASES
153  |  ADRB1  |  2.251  |  DISEASES
653  |  BMP5  |  2.316  |  DISEASES
390259  |  BSX  |  2.855  |  DISEASES
1066  |  CES1  |  1.66  |  DISEASES
1201  |  CLN3  |  1.857  |  DISEASES
594855  |  CPLX3  |  3.375  |  DISEASES
78987  |  CRELD1  |  2.948  |  DISEASES
115908  |  CTHRC1  |  2.25  |  DISEASES
79813  |  EHMT1  |  2.183  |  DISEASES
3266  |  ERAS  |  4.474  |  DISEASES
2113  |  ETS1  |  1.947  |  DISEASES
132884  |  EVC2  |  2.889  |  DISEASES
2153  |  F5  |  1.395  |  DISEASES
2303  |  FOXC2  |  2.619  |  DISEASES
2300  |  FOXL1  |  3.565  |  DISEASES
9573  |  GDF3  |  2.255  |  DISEASES
2875  |  GPT  |  1.959  |  DISEASES
3055  |  HCK  |  2.234  |  DISEASES
8091  |  HMGA2  |  1.682  |  DISEASES
3702  |  ITK  |  1.448  |  DISEASES
55784  |  MCTP2  |  3.356  |  DISEASES
4239  |  MFAP4  |  2.76  |  DISEASES
4524  |  MTHFR  |  1.397  |  DISEASES
4624  |  MYH6  |  1.461  |  DISEASES
4625  |  MYH7  |  1.357  |  DISEASES
1482  |  NKX2-5  |  3.902  |  DISEASES
5053  |  PAH  |  1.318  |  DISEASES
5095  |  PCCA  |  1.984  |  DISEASES
9752  |  PCDHA9  |  4.684  |  DISEASES
5294  |  PIK3CG  |  1.257  |  DISEASES
56342  |  PPAN  |  2.19  |  DISEASES
56980  |  PRDM10  |  1.074  |  DISEASES
9536  |  PTGES  |  2.006  |  DISEASES
5799  |  PTPRN2  |  1.561  |  DISEASES
23543  |  RBFOX2  |  2.571  |  DISEASES
6093  |  ROCK1  |  1.19  |  DISEASES
5265  |  SERPINA1  |  1.406  |  DISEASES
27244  |  SESN1  |  2.739  |  DISEASES
653509  |  SFTPA1  |  2.124  |  DISEASES
729238  |  SFTPA2  |  1.918  |  DISEASES
8243  |  SMC1A  |  1.97  |  DISEASES
150572  |  SMYD1  |  3.284  |  DISEASES
9298  |  SNORD31  |  3.444  |  DISEASES
7137  |  TNNI3  |  2.308  |  DISEASES
7247  |  TSN  |  2.173  |  DISEASES
Locus
Symbol | Locus(Total Locus:2)
NKX2-5  |  5q34
GJA1  |  6q22.31
Disease ID 8
Disease hypoplastic left heart syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:9)
HP:0002916  |  Abnormality of chromosome segregation
HP:0011560  |  Mitral atresia
HP:0004383  |  Underdeveloped left heart
HP:0001643  |  Patent ductus arteriosus
HP:0009800  |  Maternal diabetes
HP:0001718  |  Mitral stenosis
HP:0012304  |  Hypoplastic aortic arch
HP:0004383  |  Hypoplastic left heart
HP:0001631  |  Atrial septal defect
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:29)
Disease ID 8
Disease hypoplastic left heart syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:21)
C2609313  |  pericardial adhesions
C1550639  |  fistula
C0920157  |  mesenteric ischemia
C0876993  |  ventricular thrombosis
C0741299  |  atrial thrombus
C0700095  |  neuroblastoma
C0340766  |  venous hypertension
C0265881  |  hypoplastic aortic arch
C0265800  |  congenital pulmonary lymphangiectasis
C0042373  |  vascular disease
C0040961  |  tricuspid valve regurgitation
C0040961  |  tricuspid regurgitation
C0025958  |  microcephaly
C0024141  |  le syndrome
C0021308  |  infarction
C0019570  |  hirschsprung's disease
C0018817  |  atrial septal defect
C0018801  |  heart failure
C0005779  |  coagulopathy
C0005411  |  biliary atresia
C0003504  |  aortic insufficiency
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs104893965NA2697GJA1umls:C0152101CLINVARNA0.482367032NAGJA16121447974GA
rs2227885NA2697GJA1umls:C0152101CLINVARNA0.482367032NAGJA16121447932GA
rs2227885114704902697GJA1umls:C0152101UNIPROTIdentification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).0.4823670322001GJA16121447932GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:6)
HP ID HP Name MP ID MP Name Annotation
HP:0001643Patent ductus arteriosusMP:0011662persistent truncus arteriosus type iicomplete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development; type II is characterized by separate but proximate origins of the left and right pulmonary arterial branches fro
HP:0009800Maternal diabetesMP:0004803increased susceptibility to autoimmune diabetesgreater likelihood that an organism will develop inflammatory pancreatic disease resulting from the body attacking and destroying the insulin-producing beta islet cells of the pancreas
HP:0004383Hypoplastic left heartMP:0012515abnormal heart apex morphologyany structural anomaly of the lowest superficial part of the heart, normally directed downward, forward, and to the left, and overlapped by the left lung and pleura; the heart apex is formed by the inferolateral part of the left ventricle and responsible
HP:0002916Abnormality of chromosome segregationMP:0012069abnormal horizontal basal cell of olfactory epithelium morphologyany structural anomaly of the flat or angular epithelial cell with condensed nuclei and darkly staining cytoplasm containing numerous intermediate filaments inserted into desmosomes contacting surrounding supporting cells, that lie in contact with the bas
HP:0001718Mitral stenosisMP:0006117aortic valve stenosisabnormal narrowing of the aortic valve
HP:0001631Atria septal defectMP:0011667double outlet right ventricle with atrioventricular septal defecta form of DORV in which there is also a complete atrioventricular canal
Mapped by homologous gene(Total Items:7)
HP ID HP Name MP ID MP Name Annotation
HP:0011560Mitral atresiaMP:0013781abnormal mammary gland luminal epithelium morphologyany structural anomaly of the inner cell layer of the mammary epithelium bilayer that lines the luminal surface of mammary gland ducts and alveoli; luminal cells have only limited contact with the underlying basement membrane and surrounding connective ti
HP:0002916Abnormality of chromosome segregationMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0009800Maternal diabetesMP:0020101abnormal hepatic glucose productionan anomaly in the production of glucose in the liver
HP:0001631Atria septal defectMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0001718Mitral stenosisMP:0020039increased bone ossificationincrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0004383Hypoplastic left heartMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0001643Patent ductus arteriosusMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
Disease ID 8
Disease hypoplastic left heart syndrome
Case(Waiting for update.)