DiseaseID 29362
孤立性心室心肌致密化不全
Isolated Noncompaction Of The Ventricular Myocardium
MSH2017_2016_08_12:Rare congenital cardiomyopathies characterized by the lack of left ventricular myocardium compaction. The noncompaction results in numerous prominent trabeculations and a loose myocardial meshwork (spo
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Disease: 1Symptom: 2Target: 2Links: 4
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29362
- Core Entity Id
- 121930
- Source Entity Count
- 1
- Preferred Name
- Isolated Noncompaction Of The Ventricular Myocardium
- Name Cn
- 孤立性心室心肌致密化不全
- Name Pinyin
- Gu Li Xing Xin Shi Xin Ji Zhi Mi Hua Bu Quan
- Name En
- Isolated Noncompaction Of The Ventricular Myocardium
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:Rare congenital cardiomyopathies characterized by the lack of left ventricular myocardium compaction. The noncompaction results in numerous prominent trabeculations and a loose myocardial meshwork (spongy myocardium) in the LEFT VENTRICLE. Heterogeneous clinical features include diminished systolic function sometimes associated with left ventricular dilation, that presents either neonatally or progressively. Often, the RIGHT VENTRICLE is also affected. CONGESTIVE HEART FAILURE; PULMONARY EMBOLISM; and ventricular ARRHYTHMIA are commonly seen.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Isolated Noncompaction Of The Ventricular Myocardium
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Me Sh
D056830
Umls
C2717907
Sym Map
SMDE10100
Itcmdb Generated
ITX-DISEASE-E710E4EB7F91
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
MSH2017_2016_08_12:Rare congenital cardiomyopathies characterized by the lack of left ventricular myocardium compaction. The noncompaction results in numerous prominent trabeculations and a loose myocardial meshwork (spongy myocardium) in the LEFT VENTRICLE. Heterogeneous clinical features include diminished systolic function sometimes associated with left ventricular dilation, that presents either neonatally or progressively. Often, the RIGHT VENTRICLE is also affected. CONGESTIVE HEART FAILURE; PULMONARY EMBOLISM; and ventricular ARRHYTHMIA are commonly seen.