DiseaseID 5280
颅动脉炎
disease
Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.
Relationship Network
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Disease: 1Herb: 1Symptom: 12Target: 24Links: 37
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5280
- Core Entity Id
- 61754
- Source Entity Count
- 1
- Preferred Name
- Cranial Arteritis
- Name Cn
- 颅动脉炎
- Name Pinyin
- Lu Dong Mai Yan
- Name En
- Cranial Arteritis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Skin and Connective Tissue DiseasesCardiovascular Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Skin and Connective Tissue Diseases; Cardiovascular DiseasesSkin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cranial Arteritis
Role
preferred
Name
Giant Cell Arteritis
Role
preferred
Name
Juvenile Temporal Arteritis
Role
preferred
Name
Polyarteritis Nodosa
Role
preferred
Name
Temporal Arteritis
Role
preferred
Name
Necrotizing Arteritis
Role
preferred
Name
Horton Disease
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002348HBDIS002913HBDIS010149HBDIS018583HBDIS018584
Me Sh
D010488D013700
Omim
187360
Umls
C0031036C0039483C0751547C1956390C1956391
Icd10
M30.0M31.6
Med Dra
1001825010043207
Sym Map
SMDE02513SMDE07604SMDE10139SMDE12269SMDE13820
Do Class
DOID:7
Dis Ge Net
C0031036C0039483C0553548C1956390C1956391
Orphanet
397
Umls Sty
T047
Me Sh Class
C10C14C17C20
Etcm Disease
Juvenile Temporal Arteritis
Tcmbank Disease
131602175247542870830277
Itcmdb Generated
ITX-DISEASE-00FF9CD9BA0FITX-DISEASE-18480489945DITX-DISEASE-CAA6B097B4C7ITX-DISEASE-F8955DF3F1BB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Juvenile Temporal Arteritis Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Juvenile Temporal Arteritis
Global Category
Rare diseases
Anatomical Category
Bone diseases;Cardiovascular diseases;Muscle diseases;Nephrological diseases;Neuronal diseases
Disease Definition
Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.NCI2016_02D:An autoimmune, systemic, giant cell granulomatous arteritis predominantly involving the arteries that supply blood to the central nervous system, head and eyes. Superficial arteries of the scalp that are involved tend to be enlarged and tender. Signs and symptoms include headaches, myalgias, visual disturbances, and skin necrosis.|CSP2006:subacute, granulomatous arteritis involving the external carotid arteries, especially the temporal artery; occurs in elderly persons and may be manifested by constitutional symptoms, particularly severe headache, and sometimes sudden unilateral blindness; shares many of the symptoms of polymyalgia rheumatica.NCI2016_NICHD_1602D:A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative.|NCI2016_02D:A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative.|MSH2017_2016_08_12:A form of necrotizing non-granulomatous inflammation occurring primarily in medium-sized ARTERIES, often with microaneurysms. It is characterized by muscle, joint, and abdominal pain resulting from arterial infarction and scarring in affected organs. Polyarteritis nodosa with lung involvement is called CHURG-STRAUSS SYNDROME.|CSP2006:form of necrotizing vasculitis involving small- and medium-sized arteries; signs and symptoms result from infarction and scarring of the affected organ system.
Me Sh Disease Class
Cardiovascular Diseases; Skin and Connective Tissue DiseasesCardiovascular Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Skin and Connective Tissue Diseases; Cardiovascular DiseasesSkin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome