Hypotension
Symptom Information:
Symptom ID: | HPO:0002615 | |||||||||||||||||||||||||||||||||||||||||||
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) Hypotension(HPO:0002615) MedDRA: Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) Vascular tests NEC (incl blood pressure)(MedDRA:10047110) Hypotension(HPO:0002615) Vascular disorders(MedDRA:10047065) Decreased and nonspecific blood pressure disorders and shock(MedDRA:10011954) Vascular hypotensive disorders(MedDRA:10057181) Hypotension(HPO:0002615) |
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Database Frequency: | 52 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
ANALBUMINEMIA | (OMIM:616000) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alexander disease | (Orphanet:58) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
CHROMOSOME 5q12 DELETION SYNDROME | (OMIM:615668) |
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
Cardiomyopathy, familial restrictive, 3 | (OMIM:612422) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Chuvash erythrocytosis | (Orphanet:238557) |
Classic Bartter syndrome | (Orphanet:93605) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Congenital hypothyroidism | (Orphanet:442) |
Corticosteroid-binding globulin deficiency | (Orphanet:199247) |
Cutaneous mastocytosis | (Orphanet:66646) |
Dengue fever | (Orphanet:99828) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Encephalopathy due to hydroxykynureninuria | (Orphanet:79155) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypoaldosteronism | (Orphanet:427) |
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | (Orphanet:439854) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hydatidosis | (Orphanet:400) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Infant botulism | (Orphanet:178478) |
King-Denborough syndrome | (Orphanet:99741) |
Legionellosis | (Orphanet:549) |
Malignant hyperthermia | (Orphanet:423) |
Mastocytosis | (Orphanet:98292) |
Metachromatic leukodystrophy | (Orphanet:512) |
Multifocal atrial tachycardia | (Orphanet:3282) |
Neonatal hemochromatosis | (Orphanet:446) |
Neuroferritinopathy | (Orphanet:157846) |
Nipah virus disease | (Orphanet:99825) |
Perry syndrome | (Orphanet:178509) |
Primary systemic amyloidosis | (Orphanet:314701) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |
Renal tubular dysgenesis | (Orphanet:3033) |
Scrub typhus | (Orphanet:83317) |
Secondary polycythemia | (Orphanet:98428) |
Systemic capillary leak syndrome | (Orphanet:188) |
Tako-Tsubo cardiomyopathy | (Orphanet:66529) |
Whipple disease | (Orphanet:3452) |
Yellow fever | (Orphanet:99829) |
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL | (OMIM:261740) |