Headache

Symptom Information:

Symptom ID: HPO:0002315
Synonyms:
Headaches [HPO:0002315]
Headache (finding) [Orphanet:43100]
Headache [Orphanet:43100]
Headache [OMIM:Headache]
Headaches [OMIM:Headaches]
Facial pain/cephalalgia/migraine [Orphanet:43100]
Headache [MedDRA:10019211]
Cephalalgia [MedDRA:10019211]
Cephalalgia or cephalgia [MedDRA:10019211]
Cephalgia [MedDRA:10019211]
Forehead headache [MedDRA:10019211]
Fullness head [MedDRA:10019211]
Head fullness [MedDRA:10019211]
Head pain [MedDRA:10019211]
Head pressure [MedDRA:10019211]
Head throbbing [MedDRA:10019211]
Headache (except migraine) aggravated [MedDRA:10019211]
Headache discomfort [MedDRA:10019211]
Headache dull [MedDRA:10019211]
Headache fullness [MedDRA:10019211]
Headache NOS [MedDRA:10019211]
Headache NOS aggravated [MedDRA:10019211]
Headache occurring [MedDRA:10019211]
Headache temporal [MedDRA:10019211]
Headache transient [MedDRA:10019211]
Hemicephalgia [MedDRA:10019211]
Hemicrania [MedDRA:10019211]
Nocturnal headache [MedDRA:10019211]
Pain head [MedDRA:10019211]
Pounding in head [MedDRA:10019211]
Temporal headache [MedDRA:10019211]
Headache aggravated [MedDRA:10019211]
Frontal headache [MedDRA:10019211]
Occipital headache [MedDRA:10019211]
Parietal headache [MedDRA:10019211]
Headache unilateral [MedDRA:10019211]
Drug-induced headache [MedDRA:10019211]
Frequent headaches [MedDRA:10019211]
Chronic headaches [MedDRA:10019211]
Headache (excl migraine) aggravated [MedDRA:10019211]
Throbbing headache [MedDRA:10019211]
Intermittent headache [MedDRA:10019211]
Retroauricular pain [MedDRA:10019211]
Headache recurrent [MedDRA:10019211]
Hemicephalalgia [MedDRA:10019211]
Ice pick headache [MedDRA:10019211]
Chronic headaches [OMIM:Chronic headaches]
Frequent headaches [OMIM:Frequent headaches]
Frontal headache [OMIM:Frontal headache]
Headache, occipital [OMIM:Headache, occipital]
Recurrent headaches [OMIM:Recurrent headaches]
Temporal headache [OMIM:Temporal headache]
Facial pain [MedDRA:10016059]
Pain in face (finding) [Orphanet:43100]
Face ache (finding) [Orphanet:43100]
Facial Pain [Orphanet:43100]
Facial pain [OMIM:Facial pain]
Headaches [MedDRA:10019231]
Quality:
Cross references:
Orphanet:43100 "Facial pain/cephalalgia/migraine" [Orphanet:43100]
OMIM: "Headache" [OMIM:Headache]
OMIM: "Headaches" [OMIM:Headaches]
OMIM: "Chronic headaches" [OMIM:Chronic headaches]
OMIM: "Frequent headaches" [OMIM:Frequent headaches]
OMIM: "Frontal headache" [OMIM:Frontal headache]
OMIM: "Headache, occipital" [OMIM:Headache, occipital]
OMIM: "Recurrent headaches" [OMIM:Recurrent headaches]
OMIM: "Temporal headache" [OMIM:Temporal headache]
OMIM: "Facial pain" [OMIM:Facial pain]
UMLS:C0018681 "Headache" [HPO:0002315]
UMLS:C0018681 "Headache" [Orphanet:43100]
UMLS:C0015468 "Facial Pain" [Orphanet:43100]
Is a (Direct Parents):
MedDRA Nervous system disorders
HPO         Abnormality of nervous system physiology
Orphanet Functional anomalies of the nervous system
MedDRA Headaches NEC
Orphanet Migraine
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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Headache(HPO:0002315)
Database Frequency: 175 / 7739
Resource:

All diseases associated with this symptom:

ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS (OMIM:108050)
ATTRV122I amyloidosis (Orphanet:85451)
Acromegaly (Orphanet:963)
Acroosteolysis, dominant type (Orphanet:955)
Adiposis dolorosa (Orphanet:36397)
Alport syndrome (Orphanet:63)
Alveolar echinococcosis (Orphanet:284)
Arachnoiditis (Orphanet:137817)
Arnold-Chiari malformation type I (Orphanet:268882)
Arnold-Chiari malformation type II (Orphanet:1136)
Atypical teratoid tumor (Orphanet:99966)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Autosomal dominant osteopetrosis type 1 (Orphanet:2783)
Babesiosis (Orphanet:108)
Behçet disease (Orphanet:117)
Benign adult familial myoclonic epilepsy (Orphanet:86814)
Benign familial infantile seizures (Orphanet:306)
Blackfan-Diamond anemia (Orphanet:124)
Brain calcification, Rajab type (Orphanet:178506)
CADASIL (Orphanet:136)
CEREBRAL CAVERNOUS MALFORMATIONS (OMIM:116860)
CEREBRAL CAVERNOUS MALFORMATIONS 2 (OMIM:603284)
CEREBRAL CAVERNOUS MALFORMATIONS 3 (OMIM:603285)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
CINCA syndrome (Orphanet:1451)
COMPLEX I, SUBUNIT ND2 (OMIM:516001)
COMPLEX I, SUBUNIT ND5 (OMIM:516005)
COMPLEX I, SUBUNIT ND6 (OMIM:516006)
COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I (OMIM:516030)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
CYTOCHROME b OF COMPLEX III (OMIM:516020)
CYTOCHROME c OXIDASE III (OMIM:516050)
Camurati-Engelmann disease (Orphanet:1328)
Carney triad (Orphanet:139411)
Caudal regression sequence (Orphanet:3027)
Central diabetes insipidus (Orphanet:178029)
Chuvash erythrocytosis (Orphanet:238557)
Cold agglutinin disease (Orphanet:56425)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Craniodiaphyseal dysplasia (Orphanet:1513)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cushing disease (Orphanet:96253)
Cutaneous mastocytoma (Orphanet:79455)
Cutaneous mastocytosis (Orphanet:66646)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Deafness - lymphedema - leukemia (Orphanet:3226)
Dengue fever (Orphanet:99828)
Drug-induced autoimmune hemolytic anemia (Orphanet:90037)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS (OMIM:600907)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granuloma (Orphanet:99871)
Episodic ataxia type 1 (Orphanet:37612)
Episodic ataxia type 3 (Orphanet:79135)
Fabry disease (Orphanet:324)
Familial advanced sleep-phase syndrome (Orphanet:164736)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial atrial myxoma (Orphanet:615)
Familial caudal dysgenesis (Orphanet:1768)
Familial cold urticaria (Orphanet:47045)
Familial sick sinus syndrome (Orphanet:166282)
Familial thrombocytosis (Orphanet:71493)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Giant cell arteritis (Orphanet:397)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Granulomatosis with polyangiitis (Orphanet:900)
HERNS syndrome (Orphanet:63261)
HYPEROSTOSIS CORTICALIS GENERALISATA (OMIM:239100)
HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA (OMIM:145590)
HYPOMAGNESEMIA 6, RENAL (OMIM:613882)
Hartnup syndrome (Orphanet:2116)
Hemochromatosis type 3 (Orphanet:225123)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary cerebral cavernous malformation (Orphanet:221061)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Hereditary cerebral hemorrhage with amyloidosis, Italian type (Orphanet:324713)
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type (Orphanet:324703)
Hereditary continuous muscle fiber activity (Orphanet:972)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hughes-Stovin syndrome (Orphanet:228116)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydatidosis (Orphanet:400)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hyperostosis corticalis generalisata (Orphanet:3416)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hypouricemia, renal, 1 (OMIM:220150)
Hypouricemia, renal, 2 (OMIM:612076)
Immunoglobulin A vasculitis (Orphanet:761)
Indolent systemic mastocytosis (Orphanet:98848)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Insulin-resistance syndrome type A (Orphanet:2297)
Kawasaki disease (Orphanet:2331)
Kerion celsi (Orphanet:499)
L1 syndrome (Orphanet:275543)
LEUKOENCEPHALOPATHY WITH ATAXIA (OMIM:615651)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lhermitte-Duclos disease (Orphanet:65285)
Lujo hemorrhagic fever (Orphanet:319213)
Lyme disease (Orphanet:91546)
MELAS (Orphanet:550)
MONOSODIUM GLUTAMATE SENSITIVITY (OMIM:231630)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Majeed syndrome (Orphanet:77297)
Malignant atrophic papulosis (Orphanet:679)
Marburg hemorrhagic fever (Orphanet:99826)
Marshall syndrome with periodic fever (Orphanet:42642)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple endocrine neoplasia type 2 (Orphanet:653)
NLRP12-associated hereditary periodic fever syndrome (Orphanet:247868)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Nephronophthisis 2 (OMIM:602088)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 2 (Orphanet:637)
Nipah virus disease (Orphanet:99825)
Non-polyposis Turcot syndrome (Orphanet:99817)
Norrie disease (Orphanet:649)
Ornithine transcarbamylase deficiency (Orphanet:664)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteosclerosis - developmental delay - craniosynostosis (Orphanet:178377)
PARIETAL FORAMINA (OMIM:168500)
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 (OMIM:615399)
Parietal foramina (Orphanet:60015)
Parkes Weber syndrome (Orphanet:90307)
Paroxysmal cold hemoglobinuria (Orphanet:90035)
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity (Orphanet:53583)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Peripartum cardiomyopathy (Orphanet:563)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polycythemia vera (Orphanet:729)
Pontiac fever (Orphanet:99748)
Primary familial polycythemia (Orphanet:90042)
Proximal renal tubular acidosis (Orphanet:47159)
Rabies (Orphanet:770)
Rabson-Mendenhall syndrome (Orphanet:769)
Recessive hereditary methemoglobinemia type 1 (Orphanet:139373)
Recessive hereditary methemoglobinemia type 2 (Orphanet:139380)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Rhabdoid tumor (Orphanet:69077)
Rheumatic fever (Orphanet:3099)
Rift valley fever (Orphanet:319251)
SCLEROSTEOSIS 1 (OMIM:269500)
Saethre-Chotzen syndrome (Orphanet:794)
Scheie syndrome (Orphanet:93474)
Sclerosteosis (Orphanet:3152)
Scrub typhus (Orphanet:83317)
Secondary polycythemia (Orphanet:98428)
Sirenomelia (Orphanet:3169)
Sneddon syndrome (Orphanet:820)
Sweet syndrome (Orphanet:3243)
Syringomyelia (Orphanet:3280)
Systemic mastocytosis (Orphanet:2467)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Thymic tumor (Orphanet:100100)
Typhoid (Orphanet:99745)
VIBRATORY ANGIOEDEMA (OMIM:193050)
Viral hemorrhagic fever (Orphanet:341)
Von Hippel-Lindau disease (Orphanet:892)
Waldenström macroglobulinemia (Orphanet:33226)
Wilson disease (Orphanet:905)
Wolfram syndrome 1 (OMIM:222300)
Wyburn-Mason syndrome (Orphanet:53719)
Yellow fever (Orphanet:99829)