Hypertension

Symptom Information:

Symptom ID: HPO:0000822
Synonyms:
Elevated blood pressure [HPO:0000822]
Increased blood pressure [HPO:0000822]
Systemic hypertension [HPO:0000822]
Hypertensive disorder, systemic arterial (disorder) [Orphanet:35180]
Hypertensive disease [Orphanet:35180]
Hypertension [OMIM:Hypertension]
Systemic hypertension [OMIM:Systemic hypertension]
Chronic arterial hypertension [Orphanet:35180]
Hypertension [Orphanet:35180]
Hypertension [MedDRA:10020772]
Blood pressure high [MedDRA:10020772]
Blood pressure increased refractory [MedDRA:10020772]
HBP [MedDRA:10020772]
HT [MedDRA:10020772]
Hypertension aggravated [MedDRA:10020772]
Hypertension arterial [MedDRA:10020772]
Hypertension complicating pregnancy, childbirth, and the puerperium [MedDRA:10020772]
Hypertension exacerbated [MedDRA:10020772]
Hypertension NOS [MedDRA:10020772]
Hypertension not adequately controlled [MedDRA:10020772]
Hypertension paroxysmal [MedDRA:10020772]
Hypertension worsened [MedDRA:10020772]
Hypertensive [MedDRA:10020772]
Hypertensive episode [MedDRA:10020772]
Hypertensive episodes [MedDRA:10020772]
Increased BP slipping out of control [MedDRA:10020772]
Other pre-existing hypertension complicating pregnancy, childbirth, and the puerperium [MedDRA:10020772]
Other pre-existing hypertension complicating pregnancy, childbirth, and the puerperium, unspecified [MedDRA:10020772]
Other pre-existing hypertension, antepartum [MedDRA:10020772]
Other pre-existing hypertension, postpartum [MedDRA:10020772]
Other pre-existing hypertension, with delivery [MedDRA:10020772]
Other pre-existing hypertension, with delivery, with mention of postpartum complication [MedDRA:10020772]
Refractory hypertension [MedDRA:10020772]
Uncomplicated hypertension [MedDRA:10020772]
Unspec hypertension comp preg,childbirth, or the puerperium, unspec as to eoc [MedDRA:10020772]
Unspecified antepartum hypertension [MedDRA:10020772]
Unspecified hypertension complicating pregnancy, childbirth, or the puerperium [MedDRA:10020772]
Unspecified hypertension complicating pregnancy, childbirth, or the puerperium, unspecified as to ep [MedDRA:10020772]
Unspecified hypertension, with delivery [MedDRA:10020772]
Unspecified hypertension, with delivery, with mention of postpartum complication [MedDRA:10020772]
Unspecified postpartum hypertension [MedDRA:10020772]
White coat hypertension [MedDRA:10020772]
Borderline hypertension [MedDRA:10020772]
Uncontrolled hypertension [MedDRA:10020772]
Arterial hypertension (in 1 patient) [OMIM:Arterial hypertension (in 1 patient)]
Hypertension (1 family) [OMIM:Hypertension (1 family)]
Hypertension (HCP) [OMIM:Hypertension (HCP)]
Hypertension (compression of renal arteries) [OMIM:Hypertension (compression of renal arteries)]
Hypertension (especially in atypical hemolytic-uremic syndrome (aHUS)) [OMIM:Hypertension (especially in atypical hemolytic-uremic syndrome (aHUS))]
Hypertension (in some patients) [OMIM:Hypertension (in some patients)]
Hypertension (reported in 1 patient) [OMIM:Hypertension (reported in 1 patient)]
Hypertension (suppressible by glucocorticoid treatment) [OMIM:Hypertension (suppressible by glucocorticoid treatment)]
Hypertension (variable) [OMIM:Hypertension (variable)]
Hypertension (with pheochromocytoma) [OMIM:Hypertension (with pheochromocytoma)]
No hypertension [OMIM:No hypertension]
Blood pressure increased [MedDRA:10005750]
Quality:
Cross references:
Orphanet:35180 "Chronic arterial hypertension" [Orphanet:35180]
OMIM: "Hypertension" [OMIM:Hypertension]
OMIM: "Systemic hypertension" [OMIM:Systemic hypertension]
OMIM: "Arterial hypertension (in 1 patient)" [OMIM:Arterial hypertension (in 1 patient)]
OMIM: "Hypertension (1 family)" [OMIM:Hypertension (1 family)]
OMIM: "Hypertension (HCP)" [OMIM:Hypertension (HCP)]
OMIM: "Hypertension (compression of renal arteries)" [OMIM:Hypertension (compression of renal arteries)]
OMIM: "Hypertension (especially in atypical hemolytic-uremic syndrome (aHUS))" [OMIM:Hypertension (especially in atypical hemolytic-uremic syndrome (aHUS))]
OMIM: "Hypertension (in some patients)" [OMIM:Hypertension (in some patients)]
OMIM: "Hypertension (reported in 1 patient)" [OMIM:Hypertension (reported in 1 patient)]
OMIM: "Hypertension (suppressible by glucocorticoid treatment)" [OMIM:Hypertension (suppressible by glucocorticoid treatment)]
OMIM: "Hypertension (variable)" [OMIM:Hypertension (variable)]
OMIM: "Hypertension (with pheochromocytoma)" [OMIM:Hypertension (with pheochromocytoma)]
OMIM: "No hypertension" [OMIM:No hypertension]
UMLS:C0020538 "Hypertension" [HPO:0000822]
UMLS:C0020538 "Hypertensive disease" [Orphanet:35180]
Is a (Direct Parents):
MedDRA Vascular tests NEC (incl blood pressure)
HPO         Abnormality of cardiovascular system physiology
MedDRA Vascular hypertensive disorders NEC
Orphanet Abnormality of cardiovascular system physiology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Hypertension(HPO:0000822)
MedDRA:
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       Vascular tests NEC (incl blood pressure)(MedDRA:10047110)
          Hypertension(HPO:0000822)
Vascular disorders(MedDRA:10047065)
    Vascular hypertensive disorders(MedDRA:10057166)
       Vascular hypertensive disorders NEC(MedDRA:10020774)
          Hypertension(HPO:0000822)
Database Frequency: 224 / 7739
Resource:

All diseases associated with this symptom:

ABDOMINAL OBESITY-METABOLIC SYNDROME 3 (OMIM:615812)
ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT (OMIM:206570)
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 (OMIM:614473)
ARTERIOSCLEROSIS, SEVERE JUVENILE (OMIM:208060)
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS (OMIM:108050)
ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14 (OMIM:615378)
Acromegaly (Orphanet:963)
Acute intermittent porphyria (Orphanet:79276)
Alagille syndrome (Orphanet:52)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Alexander disease (Orphanet:58)
Alkaptonuria (Orphanet:56)
Alport syndrome (Orphanet:63)
Alström syndrome (Orphanet:64)
Apert syndrome (Orphanet:87)
Apparent mineralocorticoid excess (Orphanet:320)
Argininosuccinic aciduria (Orphanet:23)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arterial tortuosity syndrome (Orphanet:3342)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atypical hemolytic uremic syndrome (Orphanet:2134)
Atypical hemolytic uremic syndrome with B factor anomaly (Orphanet:93578)
Atypical hemolytic uremic syndrome with C3 anomaly (Orphanet:93575)
Atypical hemolytic uremic syndrome with H factor anomaly (Orphanet:93579)
Atypical hemolytic uremic syndrome with I factor anomaly (Orphanet:93580)
Atypical hemolytic uremic syndrome with MCP/CD46 anomaly (Orphanet:93576)
Atypical hemolytic uremic syndrome with anti-factor H antibodies (Orphanet:93581)
Atypical hemolytic uremic syndrome with thrombomodulin anomaly (Orphanet:217023)
Autosomal dominant Alport syndrome (Orphanet:88918)
Autosomal dominant beta2-microglobulinic amyloidosis (Orphanet:314652)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
Autosomal dominant progressive nephropathy with hypertension (Orphanet:88659)
Autosomal recessive Alport syndrome (Orphanet:88919)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 8 (OMIM:615985)
Bilateral renal agenesis (Orphanet:1848)
Blau syndrome (Orphanet:90340)
Brachydactyly - arterial hypertension (Orphanet:1276)
CADASIL (Orphanet:136)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 (OMIM:608320)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Carney complex (Orphanet:1359)
Carney triad (Orphanet:139411)
Catecholamine-producing tumor (Orphanet:717)
Caudal regression sequence (Orphanet:3027)
Choroideremia - hypopituitarism (Orphanet:1434)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Classical homocystinuria (Orphanet:394)
Cockayne syndrome (Orphanet:191)
Cogan syndrome (Orphanet:1467)
Congenital adrenal hyperplasia (Orphanet:418)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency (Orphanet:90793)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital hypothyroidism (Orphanet:442)
Congenital pulmonary veins atresia or stenosis (Orphanet:3188)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Corticosteroid-binding globulin deficiency (Orphanet:199247)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Cystic hamartoma of lung and kidney (Orphanet:2111)
Cystinuria (Orphanet:214)
Denys-Drash syndrome (Orphanet:220)
EAST syndrome (Orphanet:199343)
EPSTEIN SYNDROME (OMIM:153650)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Essential thrombocythemia (Orphanet:3318)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO (OMIM:607832)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
Familial dysautonomia (Orphanet:1764)
Familial hyperaldosteronism type 1 (Orphanet:403)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial isolated pituitary adenoma (Orphanet:314777)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Familial renal amyloidosis (Orphanet:85450)
Fibronectin glomerulopathy (Orphanet:84090)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (OMIM:601894)
GLUCOCORTICOID RESISTANCE, GENERALIZED (OMIM:615962)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Generalized arterial calcification of infancy (Orphanet:51608)
Gigantism (Orphanet:99725)
Glutaric acidemia type 3 (Orphanet:35706)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Grange syndrome (Orphanet:79094)
Granulomatosis with polyangiitis (Orphanet:900)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hemochromatosis type 3 (Orphanet:225123)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary coproporphyria (Orphanet:79273)
Hurler syndrome (Orphanet:93473)
Hypouricemia, renal, 1 (OMIM:220150)
Hypouricemia, renal, 2 (OMIM:612076)
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2 (OMIM:616069)
Idiopathic and/or familial pulmonary arterial hypertension (Orphanet:422)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
Idiopathic intracranial hypertension (Orphanet:238624)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:161950)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 (OMIM:613944)
Infant botulism (Orphanet:178478)
Insulin-resistance syndrome type A (Orphanet:2297)
Joubert syndrome 14 (OMIM:614424)
Juvenile Paget disease (Orphanet:2801)
LCAT deficiency (Orphanet:650)
Liddle syndrome (Orphanet:526)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
MELAS (Orphanet:550)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
MOYAMOYA DISEASE 6 WITH ACHALASIA (OMIM:615750)
Maternally-inherited diabetes and deafness (Orphanet:225)
Maturity-onset diabetes of the young, type 2 (OMIM:125851)
Melorheostosis with osteopoikilosis (Orphanet:1879)
Monosomy 18p (Orphanet:1598)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Multiple endocrine neoplasia type 2A (Orphanet:247698)
Myhre syndrome (Orphanet:2588)
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED (OMIM:256700)
NUCLEAR RECEPTOR SUBFAMILY 3, GROUP C, MEMBER 1 (OMIM:138040)
Nail-patella syndrome (Orphanet:2614)
Nail-patella-like renal disease (Orphanet:2613)
Nephroblastoma (Orphanet:654)
Nephronophthisis 18 (OMIM:615862)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Neuroblastoma (Orphanet:635)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Nodular regenerative hyperplasia of the liver (Orphanet:48372)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION (OMIM:166990)
Ochoa syndrome (Orphanet:2704)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 3 (OMIM:605373)
PARAGANGLIOMAS 4 (OMIM:115310)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pediatric systemic sclerosis (Orphanet:93567)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Pierson syndrome (Orphanet:2670)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polycythemia vera (Orphanet:729)
Porphyria (Orphanet:738)
Preeclampsia (Orphanet:275555)
Primary familial polycythemia (Orphanet:90042)
Primary lipodystrophy (Orphanet:90970)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Pseudohyperaldosteronism type 2 (Orphanet:88660)
Pseudohypoaldosteronism type 2 (Orphanet:757)
Pseudohypoaldosteronism type 2B (Orphanet:88939)
Pseudohypoaldosteronism type 2C (Orphanet:88940)
Pseudohypoaldosteronism type 2D (Orphanet:300525)
Pseudohypoaldosteronism type 2E (Orphanet:300530)
Pseudoxanthoma elasticum (Orphanet:758)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Rhabdoid tumor (Orphanet:69077)
Riboflavin transporter deficiency (Orphanet:97229)
Rothmund-Thomson syndrome (Orphanet:2909)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Secondary polycythemia (Orphanet:98428)
Senior-Loken syndrome (Orphanet:3156)
Senior-Loken syndrome 7 (OMIM:613615)
Sneddon syndrome (Orphanet:820)
Somatotroph adenoma (Orphanet:96256)
Spastic paraplegia - nephritis - deafness (Orphanet:2820)
Stiff person syndrome (Orphanet:3198)
Stiff skin syndrome (Orphanet:2833)
Systemic sclerosis (Orphanet:90291)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TRIMETHYLAMINURIA (OMIM:602079)
Takayasu arteritis (Orphanet:3287)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Torsade-de-pointes syndrome with short coupling interval (Orphanet:51084)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Typical hemolytic uremic syndrome (Orphanet:90038)
Von Hippel-Lindau disease (Orphanet:892)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
X-linked Alport syndrome (Orphanet:88917)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
XFE PROGEROID SYNDROME (OMIM:610965)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)