Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Headache (HP:0002315)help
..Starting node
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Migraine (HP:0002076)help
Term ID: 2076
Name: Migraine
Synonym: Intermittent migraine headaches; Migraine; Migraine headache; Migraine headaches
Definition: Migraine is a chronic neurological disorder characterized by episodic attacks of headache and associated symptoms.
Comments:
Reference: HP:0002076
Genes and Diseases:
 
       Child Nodes:
........expandMigraine with aura (HP:0002077) help
........expandMigraine without aura (HP:0002083) help

 Sister Nodes: 
..expandCluster headache (HP:0012199) help
..expandHypnic headache (HP:0012459) help
..expandOccipital neuralgia (HP:0012318) help
..expandRecurrent paroxysmal headache (HP:0002331) help
..expandTension-type headache (HP:0012228) help
..expandThunderclap headache (HP:0030907) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0002076HP:0002076Migraine0ACSF3 CL E G H19732227288ORPHA:289504Combined malonic and methylmalonic acidemiaHP:0040283 - Occasional68
HP:0002076HP:0002076Migraine0ACVRL1 CL E G H94175ORPHA:774Hereditary hemorrhagic telangiectasiaHP:0040282 - Frequent178
HP:0002076HP:0002076Migraine0ACVRL1 CL E G H94175OMIM:600376Telangiectasia, hereditary hemorrhagic, type 2.178
HP:0002076HP:0002076Migraine0ADA2 CL E G H518161839ORPHA:820Sneddon syndromeHP:0040281 - Very frequent22
HP:0002076HP:0002076Migraine0ADAMTSL1 CL E G H9294914632ORPHA:521445Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndromeHP:0040282 - Frequent
HP:0002076HP:0002076Migraine0AIP CL E G H9049358ORPHA:963AcromegalyHP:0040282 - Frequent95
HP:0002076HP:0002076Migraine0ALPK1 CL E G H8021620917OMIM:614979Splenomegaly, cytopenia, and vision loss
HP:0002076HP:0002076Migraine0AMACR CL E G H23600451OMIM:614307Alpha-methylacyl-CoA racemase deficiency.44
HP:0002076HP:0002076Migraine0AMACR CL E G H23600451ORPHA:79095Congenital bile acid synthesis defect type 444
HP:0002076HP:0002076Migraine0APP CL E G H351620ORPHA:324713ABeta amyloidosis, Italian typeHP:0040281 - Very frequent74
HP:0002076HP:0002076Migraine0APP CL E G H351620ORPHA:324703ABetaL34V amyloidosisHP:0040282 - Frequent74
HP:0002076HP:0002076Migraine0ATP1A2 CL E G H477800ORPHA:569Familial or sporadic hemiplegic migraine239
HP:0002076HP:0002076Migraine0ATP1A2 CL E G H477800OMIM:602481Migraine, familial hemiplegic, 2239
HP:0002076HP:0002076Migraine0BMPR1A CL E G H6571076ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent385
HP:0002076HP:0002076Migraine0C4A CL E G H7201323ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388ORPHA:71518Benign paroxysmal torticollis of infancyHP:0040282 - Frequent449
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388OMIM:108500Episodic ataxia, type 2.449
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388ORPHA:569Familial or sporadic hemiplegic migraine449
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388ORPHA:97Familial paroxysmal ataxiaHP:0040282 - Frequent449
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0002076HP:0002076Migraine0CACNA1A CL E G H7731388OMIM:183086Spinocerebellar ataxia 6HP:0040283 - Occasional449
HP:0002076HP:0002076Migraine0CCR1 CL E G H12301602ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0CLTRN CL E G H5739329437ORPHA:2116Hartnup diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0COL3A1 CL E G H12812201ORPHA:286Vascular Ehlers-Danlos syndromeHP:0040283 - Occasional749
HP:0002076HP:0002076Migraine0COL4A1 CL E G H12822202OMIM:175780Brain small vessel disease 1 with or without ocular anomalies.193
HP:0002076HP:0002076Migraine0COL5A1 CL E G H12892209OMIM:619329FIBROMUSCULAR DYSPLASIA, MULTIFOCAL; FMDMF660
HP:0002076HP:0002076Migraine0COPB1 CL E G H13152231OMIM:619255BARALLE-MACKEN SYNDROME; BARMACS
HP:0002076HP:0002076Migraine0COX1 CL E G H45127419ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0COX2 CL E G H45137421ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0COX3 CL E G H45147422ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0CSNK1D CL E G H14532452OMIM:615224Advanced sleep phase syndrome, familial, 22
HP:0002076HP:0002076Migraine0CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040284 - Very rare172
HP:0002076HP:0002076Migraine0DNM1L CL E G H100592973ORPHA:98673Autosomal dominant optic atrophy, classic formHP:0040284 - Very rare94
HP:0002076HP:0002076Migraine0EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 13
HP:0002076HP:0002076Migraine0ENG CL E G H20223349ORPHA:774Hereditary hemorrhagic telangiectasiaHP:0040282 - Frequent186
HP:0002076HP:0002076Migraine0ENG CL E G H20223349OMIM:187300Telangiectasia, hereditary hemorrhagic, type 1186
HP:0002076HP:0002076Migraine0EPCAM CL E G H407211529ORPHA:144Lynch syndromeHP:0040282 - Frequent170
HP:0002076HP:0002076Migraine0EPHB4 CL E G H20503395ORPHA:137667Capillary malformation-arteriovenous malformationHP:0040284 - Very rare3
HP:0002076HP:0002076Migraine0ERAP1 CL E G H5175218173ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002076HP:0002076Migraine0ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 113
HP:0002076HP:0002076Migraine0FAN1 CL E G H2290929170ORPHA:144Lynch syndromeHP:0040282 - Frequent15
HP:0002076HP:0002076Migraine0FAS CL E G H35511920ORPHA:117Behçet diseaseHP:0040281 - Very frequent59
HP:0002076HP:0002076Migraine0FGFR2 CL E G H22633689ORPHA:794Saethre-Chotzen syndromeHP:0040283 - Occasional175
HP:0002076HP:0002076Migraine0FGFR3 CL E G H22613690ORPHA:93262Crouzon syndrome-acanthosis nigricans syndromeHP:0040283 - Occasional145
HP:0002076HP:0002076Migraine0FGFR3 CL E G H22613690ORPHA:794Saethre-Chotzen syndromeHP:0040283 - Occasional145
HP:0002076HP:0002076Migraine0FRMD5 CL E G H8497828214OMIM:620094
HP:0002076HP:0002076Migraine0GABRG2 CL E G H25664087ORPHA:1945Rolandic epilepsyHP:0040283 - Occasional139
HP:0002076HP:0002076Migraine0GATA2 CL E G H26244171ORPHA:3226Deafness-lymphedema-leukemia syndromeHP:0040282 - Frequent137
HP:0002076HP:0002076Migraine0GDF2 CL E G H26584217ORPHA:774Hereditary hemorrhagic telangiectasiaHP:0040282 - Frequent8
HP:0002076HP:0002076Migraine0GP1BA CL E G H28114439ORPHA:274Bernard-Soulier syndromeHP:0040284 - Very rare23
HP:0002076HP:0002076Migraine0GP1BB CL E G H28124440ORPHA:274Bernard-Soulier syndromeHP:0040284 - Very rare8
HP:0002076HP:0002076Migraine0GP9 CL E G H28154444ORPHA:274Bernard-Soulier syndromeHP:0040284 - Very rare21
HP:0002076HP:0002076Migraine0GPR101 CL E G H8355014963ORPHA:963AcromegalyHP:0040282 - Frequent5
HP:0002076HP:0002076Migraine0GRIN2A CL E G H29034585ORPHA:1945Rolandic epilepsyHP:0040283 - Occasional434
HP:0002076HP:0002076Migraine0HLA-B CL E G H31064932ORPHA:117Behçet diseaseHP:0040281 - Very frequent4
HP:0002076HP:0002076Migraine0HLA-B CL E G H31064932ORPHA:3287Takayasu arteritisHP:0040282 - Frequent4
HP:0002076HP:0002076Migraine0HTR1A CL E G H33505286OMIM:614674Periodic fever, menstrual cycle-dependent.2
HP:0002076HP:0002076Migraine0IFNGR1 CL E G H34595439ORPHA:117Behçet diseaseHP:0040281 - Very frequent60
HP:0002076HP:0002076Migraine0IL10 CL E G H35865962ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0002076HP:0002076Migraine0IL12A CL E G H35925969ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0IL12A-AS1 CL E G H10192837649094ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0IL12B CL E G H35935970ORPHA:3287Takayasu arteritisHP:0040282 - Frequent31
HP:0002076HP:0002076Migraine0IL23R CL E G H14923319100ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002076HP:0002076Migraine0JAG1 CL E G H1826188OMIM:619574CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH; CMT2HH257
HP:0002076HP:0002076Migraine0KCNA1 CL E G H37366218ORPHA:98809Paroxysmal kinesigenic dyskinesiaHP:0040283 - Occasional145
HP:0002076HP:0002076Migraine0KCNK18 CL E G H33856719439OMIM:613656MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13; MGR134
HP:0002076HP:0002076Migraine0KLRC4 CL E G H83026377ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0KRAS CL E G H38456407ORPHA:144Lynch syndromeHP:0040282 - Frequent196
HP:0002076HP:0002076Migraine0LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040284 - Very rare75
HP:0002076HP:0002076Migraine0MEFV CL E G H42106998ORPHA:117Behçet diseaseHP:0040281 - Very frequent281
HP:0002076HP:0002076Migraine0MLH1 CL E G H42927127ORPHA:144Lynch syndromeHP:0040282 - Frequent1819
HP:0002076HP:0002076Migraine0MLH3 CL E G H270307128ORPHA:144Lynch syndromeHP:0040282 - Frequent131
HP:0002076HP:0002076Migraine0MLX CL E G H694511645ORPHA:3287Takayasu arteritisHP:0040282 - Frequent
HP:0002076HP:0002076Migraine0MSH2 CL E G H44367325ORPHA:144Lynch syndromeHP:0040282 - Frequent2162
HP:0002076HP:0002076Migraine0MSH6 CL E G H29567329ORPHA:144Lynch syndromeHP:0040282 - Frequent2232
HP:0002076HP:0002076Migraine0MVK CL E G H45987530ORPHA:343Hyperimmunoglobulinemia D with periodic feverHP:0040282 - Frequent150
HP:0002076HP:0002076Migraine0MYD88 CL E G H46157562ORPHA:33226Waldenström macroglobulinemiaHP:0040283 - Occasional9
HP:0002076HP:0002076Migraine0MYORG CL E G H5746219918OMIM:618317Basal ganglia calcification, idiopathic, 7, autosomal recessive.
HP:0002076HP:0002076Migraine0ND1 CL E G H45357455ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0ND4 CL E G H45387459ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0ND5 CL E G H45407461ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0ND6 CL E G H45417462ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0NDP CL E G H46937678ORPHA:649Norrie diseaseHP:0040283 - Occasional39
HP:0002076HP:0002076Migraine0NF1 CL E G H47637765ORPHA:9768517q11 microdeletion syndromeHP:0040282 - Frequent1952
HP:0002076HP:0002076Migraine0NFIX CL E G H47847788ORPHA:420179Malan overgrowth syndromeHP:0040283 - Occasional40
HP:0002076HP:0002076Migraine0NLRP3 CL E G H11454816400ORPHA:1451CINCA syndromeHP:0040281 - Very frequent217
HP:0002076HP:0002076Migraine0NOP56 CL E G H1052815911ORPHA:276198Spinocerebellar ataxia type 36HP:0040284 - Very rare9
HP:0002076HP:0002076Migraine0NOTCH3 CL E G H48547883OMIM:125310Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy.144
HP:0002076HP:0002076Migraine0NOTCH3 CL E G H48547883ORPHA:136Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathyHP:0040282 - Frequent144
HP:0002076HP:0002076Migraine0OPA1 CL E G H49768140ORPHA:1215Autosomal dominant optic atrophy plus syndromeHP:0040284 - Very rare214
HP:0002076HP:0002076Migraine0OPA1 CL E G H49768140ORPHA:98673Autosomal dominant optic atrophy, classic formHP:0040284 - Very rare214
HP:0002076HP:0002076Migraine0PDGFB CL E G H51558800OMIM:615483Basal ganglia calcification, idiopathic, 5.9
HP:0002076HP:0002076Migraine0PDGFRB CL E G H51598804OMIM:615007Basal ganglia calcification, idiopathic, 4HP:0040283 - Occasional28
HP:0002076HP:0002076Migraine0PEX11B CL E G H87998853OMIM:614920Peroxisome biogenesis disorder 14B4
HP:0002076HP:0002076Migraine0PGK1 CL E G H52308896ORPHA:713Glycogen storage disease due to phosphoglycerate kinase 1 deficiencyHP:0040282 - Frequent21
HP:0002076HP:0002076Migraine0PGK1 CL E G H52308896OMIM:300653Phosphoglycerate kinase 1 deficiency.21
HP:0002076HP:0002076Migraine0PIK3CA CL E G H52908975ORPHA:144Lynch syndromeHP:0040282 - Frequent162
HP:0002076HP:0002076Migraine0PMS1 CL E G H53789121ORPHA:144Lynch syndromeHP:0040282 - Frequent56
HP:0002076HP:0002076Migraine0PMS2 CL E G H53959122ORPHA:144Lynch syndromeHP:0040282 - Frequent1121
HP:0002076HP:0002076Migraine0POLG CL E G H54289179ORPHA:254892Autosomal dominant progressive external ophthalmoplegiaHP:0040284 - Very rare464
HP:0002076HP:0002076Migraine0POLG CL E G H54289179OMIM:607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis.464
HP:0002076HP:0002076Migraine0POLG CL E G H54289179ORPHA:70595Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndromeHP:0040283 - Occasional464
HP:0002076HP:0002076Migraine0POLG2 CL E G H112329180ORPHA:254892Autosomal dominant progressive external ophthalmoplegiaHP:0040284 - Very rare45
HP:0002076HP:0002076Migraine0PRORP CL E G H969219958OMIM:619737COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54; COXPD54
HP:0002076HP:0002076Migraine0PRRT2 CL E G H11247630500ORPHA:569Familial or sporadic hemiplegic migraine94
HP:0002076HP:0002076Migraine0PRRT2 CL E G H11247630500ORPHA:98809Paroxysmal kinesigenic dyskinesiaHP:0040283 - Occasional94
HP:0002076HP:0002076Migraine0PRRT2 CL E G H11247630500OMIM:605751Seizures, benign familial infantile, 2HP:0040283 - Occasional94
HP:0002076HP:0002076Migraine0RASA1 CL E G H59219871ORPHA:137667Capillary malformation-arteriovenous malformationHP:0040284 - Very rare88
HP:0002076HP:0002076Migraine0RELA CL E G H59709955ORPHA:251636EpendymomaHP:0040282 - Frequent1
HP:0002076HP:0002076Migraine0RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040284 - Very rare334
HP:0002076HP:0002076Migraine0RNASEH1 CL E G H24624318466ORPHA:329336Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathyHP:0040283 - Occasional3
HP:0002076HP:0002076Migraine0RPS20 CL E G H622410405ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent1
HP:0002076HP:0002076Migraine0RRM2B CL E G H5048417296ORPHA:329336Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathyHP:0040283 - Occasional125
HP:0002076HP:0002076Migraine0RRM2B CL E G H5048417296ORPHA:254892Autosomal dominant progressive external ophthalmoplegiaHP:0040284 - Very rare125
HP:0002076HP:0002076Migraine0SCN1A CL E G H632310585ORPHA:569Familial or sporadic hemiplegic migraine1053
HP:0002076HP:0002076Migraine0SCN1A CL E G H632310585OMIM:609634Migraine, familial hemiplegic, 31053
HP:0002076HP:0002076Migraine0SEMA4A CL E G H6421810729ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent48
HP:0002076HP:0002076Migraine0SH2B1 CL E G H2597030417ORPHA:261222Distal 16p11.2 microdeletion syndromeHP:0040283 - Occasional
HP:0002076HP:0002076Migraine0SLC1A3 CL E G H650710941ORPHA:209967Episodic ataxia type 6HP:0040283 - Occasional63
HP:0002076HP:0002076Migraine0SLC1A3 CL E G H650710941OMIM:612656Episodic ataxia, type 6.63
HP:0002076HP:0002076Migraine0SLC25A4 CL E G H29110990ORPHA:254892Autosomal dominant progressive external ophthalmoplegiaHP:0040284 - Very rare68
HP:0002076HP:0002076Migraine0SLC2A1 CL E G H651311005OMIM:601042Dystonia 9.255
HP:0002076HP:0002076Migraine0SLC2A1 CL E G H651311005OMIM:612126Glut1 deficiency syndrome 2HP:0040283 - Occasional255
HP:0002076HP:0002076Migraine0SLC6A19 CL E G H34002427960ORPHA:2116Hartnup diseaseHP:0040281 - Very frequent12
HP:0002076HP:0002076Migraine0SMAD3 CL E G H40886769ORPHA:284984Aneurysm-osteoarthritis syndromeHP:0040282 - Frequent260
HP:0002076HP:0002076Migraine0SMAD3 CL E G H40886769OMIM:613795LOEYS-DIETZ SYNDROME 3; LDS3260
HP:0002076HP:0002076Migraine0SMAD4 CL E G H40896770ORPHA:774Hereditary hemorrhagic telangiectasiaHP:0040282 - Frequent504
HP:0002076HP:0002076Migraine0SMARCAL1 CL E G H5048511102OMIM:242900Immunoosseous dysplasia, Schimke type74
HP:0002076HP:0002076Migraine0SMARCB1 CL E G H659811103ORPHA:99966Atypical teratoid rhabdoid tumorHP:0040282 - Frequent87
HP:0002076HP:0002076Migraine0SPOP CL E G H840511254OMIM:618829NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS216
HP:0002076HP:0002076Migraine0SQOR CL E G H5847220390OMIM:619221SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY; SQORD
HP:0002076HP:0002076Migraine0SRPX2 CL E G H2728630668ORPHA:1945Rolandic epilepsyHP:0040283 - Occasional50
HP:0002076HP:0002076Migraine0STARD7 CL E G H5691018063OMIM:607876Epilepsy, familial adult myoclonic, 2
HP:0002076HP:0002076Migraine0STAT4 CL E G H677511365ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0002076HP:0002076Migraine0STIM1 CL E G H678611386OMIM:185070Stormorken syndrome.31
HP:0002076HP:0002076Migraine0TGFBR2 CL E G H704811773ORPHA:144Lynch syndromeHP:0040282 - Frequent253
HP:0002076HP:0002076Migraine0TLR4 CL E G H709911850ORPHA:117Behçet diseaseHP:0040281 - Very frequent3
HP:0002076HP:0002076Migraine0TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 17
HP:0002076HP:0002076Migraine0TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndromeHP:0040283 - Occasional131
HP:0002076HP:0002076Migraine0TREX1 CL E G H1127712269ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHP:0040282 - Frequent56
HP:0002076HP:0002076Migraine0TREX1 CL E G H1127712269OMIM:192315Vasculopathy, retinal, with cerebral leukodystrophy.56
HP:0002076HP:0002076Migraine0TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNF CL E G H45587481ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNH CL E G H45647487ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNL1 CL E G H45677490ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNQ CL E G H45727495ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNS1 CL E G H45747497ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNS2 CL E G H45757498ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TRNW CL E G H45787501ORPHA:550MELASHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002076HP:0002076Migraine0TWIST1 CL E G H729112428ORPHA:794Saethre-Chotzen syndromeHP:0040283 - Occasional18
HP:0002076HP:0002076Migraine0TWNK CL E G H566521160ORPHA:254892Autosomal dominant progressive external ophthalmoplegiaHP:0040284 - Very rare113
HP:0002076HP:0002076Migraine0TWNK CL E G H566521160OMIM:271245Mitochondrial DNA depletion syndrome 7 (hepatocerebral type).113
HP:0002076HP:0002076Migraine0TWNK CL E G H566521160OMIM:607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis.113
HP:0002076HP:0002076Migraine0TWNK CL E G H566521160ORPHA:70595Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndromeHP:0040283 - Occasional113
HP:0002076HP:0002076Migraine0UBAC2 CL E G H33786720486ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002076HP:0002076Migraine0ZFTA CL E G H6599828449ORPHA:251636EpendymomaHP:0040282 - Frequent
HP:0002076HP:0002077Migraine with aura1ATP1A2 CL E G H477800ORPHA:569Familial or sporadic hemiplegic migraineHP:0040281 - Very frequent239
HP:0002076HP:0002077Migraine with aura1ATP1A2 CL E G H477800OMIM:602481Migraine, familial hemiplegic, 2.239
HP:0002076HP:0002077Migraine with aura1CACNA1A CL E G H7731388ORPHA:569Familial or sporadic hemiplegic migraineHP:0040281 - Very frequent449
HP:0002076HP:0002077Migraine with aura1CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0002076HP:0002077Migraine with aura1COL4A1 CL E G H12822202OMIM:175780Brain small vessel disease 1 with or without ocular anomalies193
HP:0002076HP:0002077Migraine with aura1CSNK1D CL E G H14532452OMIM:615224Advanced sleep phase syndrome, familial, 22
HP:0002076HP:0002083Migraine without aura1CSNK1D CL E G H14532452OMIM:615224Advanced sleep phase syndrome, familial, 22
HP:0002076HP:0002077Migraine with aura1EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 1.3
HP:0002076HP:0002083Migraine without aura1EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 1.3
HP:0002076HP:0002077Migraine with aura1ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 1.13
HP:0002076HP:0002083Migraine without aura1ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 1.13
HP:0002076HP:0002077Migraine with aura1KCNK18 CL E G H33856719439OMIM:613656MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13; MGR134
HP:0002076HP:0002083Migraine without aura1KCNK18 CL E G H33856719439OMIM:613656MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13; MGR134
HP:0002076HP:0002077Migraine with aura1NOTCH3 CL E G H48547883ORPHA:136Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathyHP:0040282 - Frequent144
HP:0002076HP:0002077Migraine with aura1PRRT2 CL E G H11247630500ORPHA:569Familial or sporadic hemiplegic migraineHP:0040281 - Very frequent94
HP:0002076HP:0002077Migraine with aura1SCN1A CL E G H632310585ORPHA:569Familial or sporadic hemiplegic migraineHP:0040281 - Very frequent1053
HP:0002076HP:0002077Migraine with aura1SCN1A CL E G H632310585OMIM:609634Migraine, familial hemiplegic, 3.1053
HP:0002076HP:0002083Migraine without aura1TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 1.7
HP:0002076HP:0002077Migraine with aura1TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 1.7
HP:0002076HP:0002077Migraine with aura1TREX1 CL E G H1127712269ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHP:0040283 - Occasional56
HP:0002076HP:0002083Migraine without aura1TREX1 CL E G H1127712269ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHP:0040283 - Occasional56


Genes (131) :ACSF3 ACVRL1 ADA2 ADAMTSL1 AIP ALPK1 AMACR APP ATP1A2 BMPR1A C4A CACNA1A CCR1 CLTRN COL3A1 COL4A1 COL5A1 COPB1 COX1 COX2 COX3 CSNK1D CYTB DEPDC5 DNM1L EDNRA ENG EPCAM EPHB4 ERAP1 ESR1 FAN1 FAS FGFR2 FGFR3 FRMD5 GABRG2 GATA2 GDF2 GP1BA GP1BB GP9 GPR101 GRIN2A HLA-B HTR1A IFNGR1 IL10 IL12A IL12A-AS1 IL12B IL23R JAG1 KCNA1 KCNK18 KLRC4 KRAS LGI1 MEFV MLH1 MLH3 MLX MSH2 MSH6 MVK MYD88 MYORG ND1 ND4 ND5 ND6 NDP NF1 NFIX NLRP3 NOP56 NOTCH3 OPA1 PDGFB PDGFRB PEX11B PGK1 PIK3CA PMS1 PMS2 POLG POLG2 PRORP PRRT2 RASA1 RELA RELN RNASEH1 RPS20 RRM2B SCN1A SEMA4A SH2B1 SLC1A3 SLC25A4 SLC2A1 SLC6A19 SMAD3 SMAD4 SMARCAL1 SMARCB1 SPOP SQOR SRPX2 STARD7 STAT4 STIM1 TGFBR2 TLR4 TNF TNFRSF1A TREX1 TRNC TRNF TRNH TRNK TRNL1 TRNQ TRNS1 TRNS2 TRNV TRNW TWIST1 TWNK UBAC2 ZFTA

Diseases (86) :ORPHA:289504 ORPHA:774 OMIM:600376 ORPHA:820 ORPHA:521445 ORPHA:963 OMIM:614979 OMIM:614307 ORPHA:79095 ORPHA:324713 ORPHA:324703 ORPHA:569 OMIM:602481 ORPHA:440437 ORPHA:117 ORPHA:71518 OMIM:108500 ORPHA:97 OMIM:141500 OMIM:183086 ORPHA:2116 ORPHA:286 OMIM:175780 OMIM:619329 OMIM:619255 ORPHA:550 OMIM:540000 OMIM:615224 ORPHA:101046 ORPHA:98673 OMIM:157300 OMIM:187300 ORPHA:144 ORPHA:137667 ORPHA:794 ORPHA:93262 OMIM:620094 ORPHA:1945 ORPHA:3226 ORPHA:274 ORPHA:3287 OMIM:614674 OMIM:619574 ORPHA:98809 OMIM:613656 ORPHA:343 ORPHA:33226 OMIM:618317 ORPHA:649 ORPHA:97685 ORPHA:420179 ORPHA:1451 ORPHA:276198 OMIM:125310 ORPHA:136 ORPHA:1215 OMIM:615483 OMIM:615007 OMIM:614920 ORPHA:713 OMIM:300653 ORPHA:254892 OMIM:607459 ORPHA:70595 OMIM:619737 OMIM:605751 ORPHA:251636 ORPHA:329336 OMIM:609634 ORPHA:261222 ORPHA:209967 OMIM:612656 OMIM:601042 OMIM:612126 ORPHA:284984 OMIM:613795 OMIM:242900 ORPHA:99966 OMIM:618829 OMIM:619221 OMIM:607876 OMIM:185070 ORPHA:32960 ORPHA:247691 OMIM:192315 OMIM:271245
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.