DiseaseID 3837
心内膜心肌纤维化
disease
Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
Relationship Network
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Disease: 1Experiment: 7Symptom: 3Target: 12Links: 22
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3837
- Core Entity Id
- 60093
- Source Entity Count
- 1
- Preferred Name
- Endomyocardial Fibrosis
- Name Cn
- 心内膜心肌纤维化
- Name Pinyin
- Xin Nei Mo Xin Ji Xian Wei Hua
- Name En
- Endomyocardial Fibrosis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the cardiovascular system
- Mesh Class Name
- Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
- Hpo Class Name
- Abnormality of the cardiovascular system
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Endomyocardial Fibrosis
Role
preferred
Name
Duchenne And Becker Muscular Dystrophy
Role
preferred
Name
Obscure African Cardiomyopathy
Role
preferred
Name
Becker Muscular Dystrophy
Role
preferred
Name
Benign Congenital Myopathy
Role
preferred
Name
Muscular Dystrophy, Duchenne
Role
preferred
Name
Duchenne Muscular Dystrophy
Role
alias
Name
Endocardial Fibrosis
Role
alias
Name
Muscular Dystrophy, Becker Type
Role
alias
Name
Muscular Dystrophy, Duchenne Type
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0006685
Herb
HBDIS000832HBDIS010176HBDIS010658HBDIS012363HBDIS018596HBDIS021650
Me Sh
D004719D020388
Omim
300376310200
Umls
C0553980C1959600C3542021
Sym Map
SMDE04335SMDE08051SMDE08287SMDE11560
Do Class
DOID:630DOID:7
Dis Ge Net
C0013264C0553980C0699741C0917713C1959600C3542021
Umls Sty
T019T046T047
Hpo Class
HP:0001626
Me Sh Class
C05C10C14C16
Tcmbank Disease
1579318362094127843281382842232249
Itcmdb Generated
ITX-DISEASE-392CCFB8034EITX-DISEASE-A3E467DB56E0ITX-DISEASE-E57030A2085D
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
01
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the cardiovascular system
Link Disease Id
853.0
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the cardiovascular system
Umls Disease Type
Disease or SyndromeDisease or Syndrome; Congenital AbnormalityPathologic Function
Disease Definition
Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.NCI2016_02D:A disease characterized by fibrotic thickening of the endocardium, particularly the right and/or left inflow tracts. The disease often involves the atrioventricular valves, leading to valvular regurgitaion. It most commonly occurs in children living within 15 degrees of the equator.|MSH2017_2016_08_12:A condition characterized by the thickening of the ventricular ENDOCARDIUM and subendocardium (MYOCARDIUM), seen mostly in children and young adults in the TROPICAL CLIMATE. The fibrous tissue extends from the apex toward and often involves the HEART VALVES causing restrictive blood flow into the respective ventricles (CARDIOMYOPATHY, RESTRICTIVE).|HPO2016_07_04:The presence of excessive connective tissue in the endocardium. [HPO:probinson]|CSP2006:disease characterized by thickening of the endocardium, and frequently the inner third of the myocardium; left ventricle is most frequently involved.
Me Sh Disease Class
Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or SyndromeDisease or Syndrome; Congenital AbnormalityPathologic Function