DiseaseID 17266
APP相关性脑淀粉样血管病
disease
Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Piedmont type is a form of HCHWA (see this term) characterized by an age of onset between 50-70 years of age, recurrent lobar intracerebral hem
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Herb: 2Symptom: 8Target: 18Links: 34
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 17266
- Core Entity Id
- 75471
- Source Entity Count
- 1
- Preferred Name
- Cerebral Amyloid Angiopathy, App-Related
- Name Cn
- APP相关性脑淀粉样血管病
- Name Pinyin
- App Xiang Guan Xing Nao Dian Fen Yang Xue Guan Bing
- Name En
- Cerebral Amyloid Angiopathy, App-Related
- 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
- genetic 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 metabolism; genetic disease
- Disease Definition
- Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Piedmont type is a form of HCHWA (see this term) characterized by an age of onset between 50-70 years of age, recurrent lobar intracerebral hem
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cerebral Amyloid Angiopathy, App-Related
Role
preferred
Name
Abeta Amyloidosis, Dutch Type
Role
preferred
Name
Abetal34V Amyloidosis
Role
preferred
Name
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
Role
preferred
Name
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
Role
preferred
Name
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
Role
preferred
Name
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
Role
preferred
Name
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
Role
preferred
Name
Amyloidosis, Cerebroarterial, App-Related
Role
alias
Name
App-Related Cerebral Amyloid Angiopathy
Role
alias
Name
Hchwad
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS019944HBDIS019948HBDIS020330HBDIS022798HBDIS022799HBDIS022800
Omim
605714
Umls
C0268394C2751494C2751536C2931672C3888307C3888308C3888309
Sym Map
SMDE00895SMDE03383SMDE04371SMDE06890
Do Class
DOID:0014667DOID:630
Dis Ge Net
C2751494C2751536C2931672C3888307C3888308C3888309
Orphanet
100006324703
Umls Sty
T047
Me Sh Class
C10C14C16C18
Etcm Disease
Cerebral Amyloid Angiopathy, App-Related
Tcmbank Disease
14768153322118247052651031252
Itcmdb Generated
ITX-DISEASE-022052DF6D4DITX-DISEASE-35A6AF9952FD
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Cerebral Amyloid Angiopathy, App-Related Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cerebral Amyloid Angiopathy, App-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), Piedmont type is a form of HCHWA (see this term) characterized by an age of onset between 50-70 years of age, recurrent lobar intracerebral hemHereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is a form of HCHWA (see this term), a group of familial central nervous system disorders, characterized by severe cerebral amyloid
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