Migraine
Symptom Information:
Symptom ID: | HPO:0002076 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Headache(HPO:0002315) Migraine(HPO:0002076) MedDRA: Nervous system disorders(MedDRA:10029205) Headache(HPO:0002315) Migraine(HPO:0002076) |
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Database Frequency: | 41 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY | (OMIM:614307) |
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT | (OMIM:206570) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 | (OMIM:615007) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 | (OMIM:615483) |
CADASIL | (Orphanet:136) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cushing disease | (Orphanet:96253) |
Episodic ataxia type 6 | (Orphanet:209967) |
Familial paroxysmal ataxia | (Orphanet:97) |
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | (Orphanet:713) |
HERNS syndrome | (Orphanet:63261) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Leber plus disease | (Orphanet:99718) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 | (OMIM:141500) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 3 | (OMIM:609634) |
PAROXYSMAL NONKINESIGENIC DYSKINESIA 2 | (OMIM:611147) |
PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT | (OMIM:614674) |
PEROXISOME BIOGENESIS DISORDER 14B | (OMIM:614920) |
PHACE syndrome | (Orphanet:42775) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Paroxysmal exertion-induced dyskinesia | (Orphanet:98811) |
Progressive hemifacial atrophy | (Orphanet:1214) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 | (OMIM:605751) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Sneddon syndrome | (Orphanet:820) |
Spinocerebellar ataxia type 6 | (Orphanet:98758) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Syringomyelia | (Orphanet:3280) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |