DiseaseID 13361
家族性脑淀粉样血管病
disease
Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Icelandic type is a form of HCHWA (see this term) characterized by an age of onset of 20-30 years, systemic amyloidosis and recurrent lobar int
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Disease: 1Formula: 18Herb: 12Symptom: 1Target: 19Links: 55
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13361
- Core Entity Id
- 70990
- Source Entity Count
- 1
- Preferred Name
- Familial Cerebral Amyloid Angiopathy
- Name Cn
- 家族性脑淀粉样血管病
- Name Pinyin
- Jia Zu Xing Nao Dian Fen Yang Xue Guan Bing
- Name En
- Familial Cerebral Amyloid Angiopathy
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- disease of metabolismgenetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolismdisease of metabolism; genetic disease
- Disease Definition
- Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Icelandic type is a form of HCHWA (see this term) characterized by an age of onset of 20-30 years, systemic amyloidosis and recurrent lobar int
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Familial Cerebral Amyloid Angiopathy
Role
preferred
Name
Cerebral Amyloid Angiopathy, Cst3-Related
Role
preferred
Name
Acys Amyloidosis
Role
preferred
Name
Cerebral Amyloid Angiopathy, Genetic
Role
preferred
Name
Cerebral Amyloid Angiopathy, Hereditary
Role
preferred
Name
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
Role
preferred
Name
AMYLOIDOSIS VI
Role
alias
Name
AMYLOIDOSIS, CEREBROARTERIAL, ICELANDIC TYPE
Role
alias
Name
CEREBRAL HEMORRHAGE, HEREDITARY, WITH AMYLOIDOSIS
Role
alias
Name
Cerebral Amyloid Angiopathy
Role
alias
Name
Cerebral Amyloid Angiopathy, Familial
Role
alias
Name
Cst3-Related Cerebral Amyloid Angiopathy
Role
alias
Name
HCHWA
Role
alias
Name
HEREDITARY CEREBRAL HEMORRHAGE WITH AMYLOIDOSIS
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS006294HBDIS014341HBDIS014453HBDIS018582
Me Sh
D028243
Omim
105150
Umls
C1510489C1527338
Sym Map
SMDE00904SMDE02364
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0268393C1510489C1527338C1956349
Orphanet
100008
Umls Sty
T047
Me Sh Class
C10C14C16C18
Etcm Disease
Cerebral Amyloid Angiopathy, Cst3-Related
Tcmbank Disease
1185015210282677280
Itcmdb Generated
ITX-DISEASE-794495EFCC85ITX-DISEASE-E8D6C0CB26AF
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Cerebral Amyloid Angiopathy, Cst3-Related Details page
Do Class Name
disease of metabolismdisease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
disease of metabolismgenetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cerebral Amyloid Angiopathy, Cst3-Related
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Bone diseases;Cardiovascular diseases;Ear diseases;Mental diseases;Muscle diseases;Neuronal diseases
Disease Definition
Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Icelandic type is a form of HCHWA (see this term) characterized by an age of onset of 20-30 years, systemic amyloidosis and recurrent lobar int
Me Sh Disease Class
Cardiovascular Diseases; Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome