DiseaseID 8809
共同心室
disease
NCI2016_NICHD_1602D:The presence of a defect (opening) in the septum that separates the two ventricles of the heart. The VSD can be congenital or acquired.|NCI2016_02D:The presence of a defect (opening) in the septum tha
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8809
- Core Entity Id
- 65793
- Source Entity Count
- 1
- Preferred Name
- Common Ventricle
- Name Cn
- 共同心室
- Name Pinyin
- Gong Tong Xin Shi
- Name En
- Common Ventricle
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesPathological Conditions, Signs and Symptoms; Nervous System Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entitygenetic disease
- Hpo Class
- Abnormality of the cardiovascular system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of the cardiovascular system
- Do Class Name
- disease of anatomical entitygenetic disease
- Disease Definition
- NCI2016_NICHD_1602D:The presence of a defect (opening) in the septum that separates the two ventricles of the heart. The VSD can be congenital or acquired.|NCI2016_02D:The presence of a defect (opening) in the septum that separates the two ventricles of the heart. It can be congenital or acquired.|MSH2017_2016_08_12:Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect.|HPO2016_07_04:A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum. [HPO:curators]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Common Ventricle
Role
preferred
Name
Thiamine-Responsive Megaloblastic Anemia Syndrome
Role
preferred
Name
Ventricular Septal Defect 1
Role
preferred
Name
Ventricular Septal Defect 2
Role
preferred
Name
Ventricular Septal Defect 3
Role
preferred
Name
Ventricular Septal Defects
Role
preferred
Name
Thiamine Responsive Megaloblastic Anemia Syndrome
Role
preferred
Name
Heart Septal Defects, Ventricular
Role
alias
Name
Hole In Heart Wall Separating Two Lower Heart Chambers
Role
alias
Name
MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUS AND SENSORINEURAL DEAFNESS
Role
alias
Name
Rogers Syndrome
Role
alias
Name
Single Ventricle
Role
alias
Name
THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA, DIABETES MELLITUS, AND DEAFNESS TYPE)
Role
alias
Name
THIAMINE-RESPONSIVE ANEMIA SYNDROME
Role
alias
Name
THIAMINE-RESPONSIVE MYELODYSPLASIA
Role
alias
Name
THMD1
Role
alias
Name
TRMA
Role
alias
Name
Thiamine-responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Deafness
Role
alias
Name
VSD1
Role
alias
Name
VSD2
Role
alias
Name
VSD3
Role
alias
Name
Ventricular Septal Defect
Role
alias
Name
Ventriculoseptal Defect
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001629HP:0001750
Herb
HBDIS001274HBDIS003722HBDIS007968HBDIS021343HBDIS021345HBDIS021346
Me Sh
D006345
Omim
249270614429614431614432
Umls
C0018818C0342287C3280777C3280783C3280785
Icd10
Q21.0
Sym Map
SMDE00067SMDE01442SMDE03849SMDE04839SMDE14250
Do Class
DOID:630DOID:7
Dis Ge Net
C0018818C0152424C0342287C3280777C3280783C3280785
Orphanet
49827
Umls Sty
T019T047
Hpo Class
HP:0001626
Me Sh Class
C09C10C14C15C16C18C19C23
Tcmbank Disease
1931426213313433756423668
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entitygenetic disease
Disease Type
diseasegroup
Hpo Class Name
Abnormality of the cardiovascular system
Do Disease Class
disease of anatomical entitygenetic disease
Hpo Disease Class
Abnormality of the cardiovascular system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome; Congenital Abnormality
Disease Definition
NCI2016_NICHD_1602D:The presence of a defect (opening) in the septum that separates the two ventricles of the heart. The VSD can be congenital or acquired.|NCI2016_02D:The presence of a defect (opening) in the septum that separates the two ventricles of the heart. It can be congenital or acquired.|MSH2017_2016_08_12:Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect.|HPO2016_07_04:A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum. [HPO:curators]Thiamine-responsive megaloblastic anemia (TRMA) is characterized by a triad of megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness.
Me Sh Disease Class
Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesPathological Conditions, Signs and Symptoms; Nervous System Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome; Congenital Abnormality