Migraine

Symptom Information:

Symptom ID: HPO:0002076
Synonyms:
Intermittent migraine headaches [HPO:0002076]
Migraine headache [HPO:0002076]
Migraine headaches [HPO:0002076]
Migraine (disorder) [Orphanet:43100]
Sick headache (disorder) [Orphanet:43100]
Migraine without aura (disorder) [Orphanet:43100]
Sick Headaches [Orphanet:43100]
Migraine Disorders [Orphanet:43100]
Intermittent migraine headaches [OMIM:Intermittent migraine headaches]
Migraine [OMIM:Migraine]
Migraine headache [OMIM:Migraine headache]
Facial pain/cephalalgia/migraine [Orphanet:43100]
Migraine [Orphanet:43100]
Migraine [MedDRA:10027599]
Fulgurating migraine [MedDRA:10027599]
Migraine aggravated [MedDRA:10027599]
Migraine headache [MedDRA:10027599]
Migraine NOS [MedDRA:10027599]
Migraine type headaches [MedDRA:10027599]
Migraine, unspecified [MedDRA:10027599]
Migraine, unspecified, with intractable migraine, so stated [MedDRA:10027599]
Migraine, unspecified, without mention of intractable migraine [MedDRA:10027599]
Migrainous headache [MedDRA:10027599]
Migrainous neuralgia [MedDRA:10027599]
Other forms of migraine [MedDRA:10027599]
Other forms of migraine with intractable migraine, so stated [MedDRA:10027599]
Other forms of migraine without mention of intractable migraine [MedDRA:10027599]
Variants of migraine [MedDRA:10027599]
Variants of migraine with intractable migraine, so stated [MedDRA:10027599]
Variants of migraine without mention of intractable migraine [MedDRA:10027599]
Confusional migraine [MedDRA:10027599]
Menstrual migraine [MedDRA:10027599]
Acute migraine [MedDRA:10027599]
Chronic migraine [MedDRA:10027599]
Migraine (40% of patients) [OMIM:Migraine (40% of patients)]
Migraine (in affected males) [OMIM:Migraine (in affected males)]
Migraine (in some patients) [OMIM:Migraine (in some patients)]
Migraine (uncommon) [OMIM:Migraine (uncommon)]
Migraine headache (less common) [OMIM:Migraine headache (less common)]
Migraine headaches (CVS+) [OMIM:Migraine headaches (CVS+)]
Migraine headaches (ipsilateral to facial hemangioma) [OMIM:Migraine headaches (ipsilateral to facial hemangioma)]
Migraine headaches (onset in adolescence) [OMIM:Migraine headaches (onset in adolescence)]
Migraines (less common) [OMIM:Migraines (less common)]
Facial pain [MedDRA:10016059]
Pain in face (finding) [Orphanet:43100]
Face ache (finding) [Orphanet:43100]
Facial Pain [Orphanet:43100]
Facial pain [OMIM:Facial pain]
Migraine headaches [MedDRA:10027603]
Migraine without aura [MedDRA:10052787]
Quality:
Cross references:
Orphanet:43100 "Facial pain/cephalalgia/migraine" [Orphanet:43100]
OMIM: "Intermittent migraine headaches" [OMIM:Intermittent migraine headaches]
OMIM: "Migraine" [OMIM:Migraine]
OMIM: "Migraine headache" [OMIM:Migraine headache]
OMIM: "Migraine (40% of patients)" [OMIM:Migraine (40% of patients)]
OMIM: "Migraine (in affected males)" [OMIM:Migraine (in affected males)]
OMIM: "Migraine (in some patients)" [OMIM:Migraine (in some patients)]
OMIM: "Migraine (uncommon)" [OMIM:Migraine (uncommon)]
OMIM: "Migraine headache (less common)" [OMIM:Migraine headache (less common)]
OMIM: "Migraine headaches (CVS+)" [OMIM:Migraine headaches (CVS+)]
OMIM: "Migraine headaches (ipsilateral to facial hemangioma)" [OMIM:Migraine headaches (ipsilateral to facial hemangioma)]
OMIM: "Migraine headaches (onset in adolescence)" [OMIM:Migraine headaches (onset in adolescence)]
OMIM: "Migraines (less common)" [OMIM:Migraines (less common)]
OMIM: "Facial pain" [OMIM:Facial pain]
UMLS:C0149931 "Migraine" [HPO:0002076]
UMLS:C0700438 "Sick Headaches" [Orphanet:43100]
UMLS:C0149931 "Migraine Disorders" [Orphanet:43100]
UMLS:C0015468 "Facial Pain" [Orphanet:43100]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Headache
HPO         Headache
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)
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)