DiseaseID 830
猝死
disease
HPO2016_07_04:Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. [HPO:probinson, pmid:17916581]|CSP2006:myocardial disease c
Relationship Network
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Disease: 1Experiment: 1Herb: 12Symptom: 12Target: 24Links: 49
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 830
- Core Entity Id
- 930
- Source Entity Count
- 2
- Preferred Name
- Sudden Death
- Name Cn
- 猝死
- Name Pinyin
- Cu Si
- Name En
- Sudden Death
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular DiseasesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and SymptomsPathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the cardiovascular system
- Mesh Class Name
- Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesPathological Conditions, Signs and SymptomsPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the cardiovascular system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- HPO2016_07_04:Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. [HPO:probinson, pmid:17916581]|CSP2006:myocardial disease characterized by general increase in bulk of the myocardium due to an increase in cell volume; it is not due to tumor formation, nor to an increase in the number of cells; involving mainly the interventricular septum, interfering with left ventricular emptying.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Sudden Death
Role
preferred
Name
Asymmetric Septal Hypertrophy
Role
preferred
Name
Cardiomyopathy, Familial Hypertrophic, 1
Role
preferred
Name
Cardiomyopathy, Hypertrophic, Familial
Role
preferred
Name
Hypertrophic Cardiomyopathy
Role
preferred
Name
Obstructive Asymmetric Septal Hypertrophy
Role
preferred
Name
Cardiomyopathy, Familial Hypertrophic, 1 (Disorder)
Role
preferred
Name
Hypertrophic Obstructive Cardiomyopathy
Role
preferred
Name
Idiopathic Hypertrophic Subaortic Stenosis
Role
preferred
Name
Primary Hypertrophic Cardiomyopathy
Role
preferred
Name
ASH
Role
alias
Name
CMH
Role
alias
Name
CMH1
Role
alias
Name
Cardiomyopathy, Hypertrophic
Role
alias
Name
Cardiomyopathy, Hypertrophic Obstructive
Role
alias
Name
Death, Sudden
Role
alias
Name
Enlarged And Thickened Heart Muscle
Role
alias
Name
Familial Hypertrophic Cardiomyopathy
Role
alias
Name
HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC
Role
alias
Name
Hypertrophic Cardiomyopathy 1
Role
alias
Name
Obstructive Hypertrophic Cardiomyopathy
Role
alias
Name
VENTRICULAR HYPERTROPHY, HEREDITARY
Role
alias
Name
Sudden death
Role
preferred
Source
TCMBank
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001639HP:0001670HP:0001699
Herb
HBDIS000469HBDIS000719HBDIS004288HBDIS010430HBDIS010670HBDIS012563HBDIS021504HBDIS027177HBDIS029432
Me Sh
D002312D003645D024741
Omim
192600590035
Umls
C0007194C0011071C0205700C0597124C0700053C0949658C3495498
Icd10
I42.1
Sym Map
SMDE04087SMDE06104SMDE06777SMDE09668SMDE11571SMDE13723
Do Class
DOID:7
Dis Ge Net
C0007194C0011071C0205700C0597124C0700053C0949658C3495498C3665332C4551472
Umls Sty
T019T046T047
Hpo Class
HP:0001626
Me Sh Class
C14C16C23
Etcm Disease
Cardiomyopathy, Familial Hypertrophic, 1
Tcmbank Disease
102743159332138420443684435444745082209685
Itcmdb Generated
ITX-DISEASE-0E89BD56E695ITX-DISEASE-24A694419129ITX-DISEASE-A74FF8CEB406ITX-DISEASE-DA686AC02E4EITX-DISEASE-F1D27A59A019
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Cardiomyopathy, Familial Hypertrophic, 1 Details page
Do Class Name
disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the cardiovascular system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the cardiovascular system
Umls Disease Type
Congenital AbnormalityDisease or SyndromePathologic Function
Basic Information
Disease Name
Cardiomyopathy, Familial Hypertrophic, 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Cardiovascular diseases;Respiratory diseases
Disease Definition
HPO2016_07_04:Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. [HPO:probinson, pmid:17916581]|CSP2006:myocardial disease characterized by general increase in bulk of the myocardium due to an increase in cell volume; it is not due to tumor formation, nor to an increase in the number of cells; involving mainly the interventricular septum, interfering with left ventricular emptying.NCI2016_02D:A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract.|MSH2017_2016_08_12:A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY).|HPO2016_07_04:Hypertrophic cardiomyopathy (HCM) is defined by the presence of increased ventricular wall thickness or mass in the absence of loading conditions (hypertension, valve disease) sufficient to cause the observed abnormality. [pmid:17916581]|CSP2006:myocardial disease characterized by hypertrophy, involving mainly the interventricular septum, interfering with left ventricular emptying.NCI2016_02D:Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.|MSH2017_2016_08_12:An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.NCI2016_CTCAE_1602D:An unexpected cessation of life that cannot be attributed to a CTCAE term associated with Grade 5.|NCI2016_02D:An unexpected death without warning.|MSH2017_2016_08_12:The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions.|HPO2016_07_04:Rapid and unexpected death. [HPO:probinson]
Me Sh Disease Class
Cardiovascular DiseasesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and SymptomsPathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesPathological Conditions, Signs and SymptomsPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or SyndromePathologic Function