Hypertension
Symptom Information:
Symptom ID: | HPO:0000822 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Hypertension(HPO:0000822) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Vascular hypertensive disorders NEC(MedDRA:10020774) Hypertension(HPO:0000822) Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) Vascular tests NEC (incl blood pressure)(MedDRA:10047110) Hypertension(HPO:0000822) |
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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) |