DiseaseID 5900
先兆性偏头痛
disease
Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the aura. Hemiplegic migraine has two main forms depending on the familial his
Relationship Network
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Disease: 1Herb: 4Symptom: 12Target: 24Links: 40
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5900
- Core Entity Id
- 62474
- Source Entity Count
- 1
- Preferred Name
- Migraine With Aura
- Name Cn
- 先兆性偏头痛
- Name Pinyin
- Xian Zhao Xing Pian Tou Tong
- Name En
- Migraine With Aura
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Nervous System DiseasesNervous System Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Nervous System DiseasesPathological Conditions, Signs and Symptoms; Nervous System Diseases
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the aura. Hemiplegic migraine has two main forms depending on the familial his
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Migraine With Aura
Role
preferred
Name
Accompaniments Migraine
Role
preferred
Name
Basilar-Type Migraine
Role
preferred
Name
Familial Hemiplegic Migraine
Role
preferred
Name
Hemiplegic Migraine, Familial Type 1
Role
preferred
Name
Migraine Triggered Seizures
Role
preferred
Name
Migraine With Prolonged Aura
Role
preferred
Name
Migraine With Typical Aura
Role
preferred
Name
Migraine, Familial Basilar
Role
preferred
Name
Migraine, Familial Hemiplegic, 1
Role
preferred
Name
Migraine, Familial Hemiplegic, 2
Role
preferred
Name
Migraine, Sporadic Hemiplegic
Role
preferred
Name
Migraines Retinal
Role
preferred
Name
Familial Or Sporadic Hemiplegic Migraine
Role
preferred
Name
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
Role
preferred
Name
Complicated Migraine
Role
alias
Name
FHM
Role
alias
Name
FHM1
Role
alias
Name
FHM2
Role
alias
Name
Familial Hemiplegic Migraine 1
Role
alias
Name
Familial Hemiplegic Migraine 2
Role
alias
Name
Hemiplegic Migraine, Familial Type 2
Role
alias
Name
MHP1
Role
alias
Name
MHP2
Role
alias
Name
MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA
Role
alias
Name
Migraine With Aura [Classical Migraine]
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002077
Herb
HBDIS003881HBDIS006519HBDIS007670HBDIS007671HBDIS014938HBDIS015122HBDIS015123HBDIS015124HBDIS018205HBDIS018206
Me Sh
D020325
Omim
141500602481
Umls
C0154723C0270860C0270861C0338483C0338484C0338486C1735856C1832884C1832903C1865322C1865323C2349436
Icd10
G43.1G43.109G43.3
Sym Map
SMDE00670SMDE00705SMDE03970SMDE05323SMDE06292SMDE08639SMDE09322SMDE10994SMDE10999SMDE11003SMDE11004SMDE11006SMDE11007SMDE11008
Do Class
DOID:7
Dis Ge Net
C0154723C0270860C0338483C0338484C1735856C1832884C1832885C1832903C1865322C1865323
Orphanet
569
Umls Sty
T033T047
Hpo Class
HP:0000707
Me Sh Class
C10C23
Etcm Disease
Familial or Sporadic Hemiplegic MigraineMigraine, Familial Hemiplegic, 1Migraine, Familial Hemiplegic, 2
Tcmbank Disease
12445130601386817990183922345226586294673086231260983
Itcmdb Generated
ITX-DISEASE-066DA35BD4C6ITX-DISEASE-28DD694BFC1BITX-DISEASE-54D5C44E5A0FITX-DISEASE-5C7A4D3EB063ITX-DISEASE-65F9675F783BITX-DISEASE-92E2DD567187ITX-DISEASE-9981E2004F64ITX-DISEASE-9A70A2DE4A11ITX-DISEASE-BDC8CDB25412ITX-DISEASE-BF7D8E0B7AACITX-DISEASE-CD69F63F2DEDITX-DISEASE-CDF728450F33ITX-DISEASE-E5340DA3FEFEITX-DISEASE-FD9C76842B1F
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Familial or Sporadic Hemiplegic Migraine Details pageDisease Migraine, Familial Hemiplegic, 1 Details pageDisease Migraine, Familial Hemiplegic, 2 Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the nervous system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the nervous system
Umls Disease Type
Disease or SyndromeFinding
Basic Information
Disease Name
Familial or Sporadic Hemiplegic Migraine
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Disease Name
Migraine, Familial Hemiplegic, 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Disease Name
Migraine, Familial Hemiplegic, 2
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Disease Definition
Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the aura. Hemiplegic migraine has two main forms depending on the familial hisNCI2016_NICHD_1602D:A migraine disorder characterized by an aura that includes motor weakness and the absence of family history.|NCI2016_02D:A migraine disorder characterized by an aura that includes motor weakness and the absence of family history.NCI2016_NICHD_1602D:A migraine disorder characterized by episodes that are preceded by focal neurological symptoms originating in the brainstem.|NCI2016_02D:A migraine disorder characterized by episodes that are preceded by focal neurological symptoms originating in the brainstem.NCI2016_NICHD_1602D:A migraine disorder characterized by episodes that are preceded by focal neurological symptoms.|NCI2016_02D:A migraine disorder characterized by episodes that are preceded by focal neurological symptoms.|MSH2017_2016_08_12:A subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)|HPO2016_07_04:A type of migraine in which there is an aura characterized by focal neurological phenomena that usually proceed, but may accompany or occur in the absence of, the headache. The symptoms of an aura may include fully reversible visual, sensory, and speech symptoms but not motor weakness. Visual symptoms may include flickering lights, spots and lines and/or loss of vision and/or unilateral sensory symptoms such as paresthesias or numbness. At least one of the symptoms of an aura develops gradually over 5 or more minutes and/or different symptoms occur in succession. [HPO:probinson, pmid:15304572]NCI2016_NICHD_1602D:A migraine disorder characterized by individual and family history of aura that includes motor weakness.|NCI2016_02D:A migraine disorder characterized by individual and family history of aura that includes motor weakness.NCI2016_NICHD_1602D:A seizure triggered by a migraine.|NCI2016_02D:A seizure triggered by a migraine.
Me Sh Disease Class
Nervous System DiseasesNervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Nervous System DiseasesPathological Conditions, Signs and Symptoms; Nervous System Diseases
Umls Semantic Type Name
Disease or SyndromeFinding