Hypotension

Symptom Information:

Symptom ID: HPO:0002615
Synonyms:
Arterial hypotension [HPO:0002615]
Low blood pressure [HPO:0002615]
Low blood pressure (disorder) [Orphanet:35240]
Hypotension [Orphanet:35240]
Arterial hypotension [OMIM:Arterial hypotension]
Hypotension [OMIM:Hypotension]
Low blood pressure [OMIM:Low blood pressure]
Blood pressure decreased [Orphanet:35240]
Blood pressure decreased [MedDRA:10005734]
Arterial blood pressure decreased [MedDRA:10005734]
Arterial pressure NOS decreased [MedDRA:10005734]
Blood pressure drop arterial [MedDRA:10005734]
Blood pressure dropped [MedDRA:10005734]
Blood pressure dropped transient [MedDRA:10005734]
BP fell [MedDRA:10005734]
BP lowered [MedDRA:10005734]
Drop in blood pressure [MedDRA:10005734]
Drop of blood pressure [MedDRA:10005734]
Fall in blood pressure [MedDRA:10005734]
Lowered blood pressure [MedDRA:10005734]
Mean blood pressure decreased [MedDRA:10005734]
Mean BP decreased [MedDRA:10005734]
Nonspecific low blood pressure reading [MedDRA:10005734]
Pressure arterial decreased [MedDRA:10005734]
Blood pressure reading low [MedDRA:10005734]
Hypotension [MedDRA:10021097]
Blood pressure low [MedDRA:10021097]
Chronic hypotension [MedDRA:10021097]
Hypotension asymptomatic [MedDRA:10021097]
Hypotension NOS [MedDRA:10021097]
Hypotension paroxysm [MedDRA:10021097]
Hypotension symptomatic [MedDRA:10021097]
Hypotension, unspecified [MedDRA:10021097]
Hypotensive [MedDRA:10021097]
Hypotensive episode [MedDRA:10021097]
Iatrogenic hypotension [MedDRA:10021097]
Low blood pressure [MedDRA:10021097]
Low BP [MedDRA:10021097]
Hypotension aggravated [MedDRA:10021097]
Acute hypotension [MedDRA:10021097]
Preshock [MedDRA:10021097]
Transient systolic hypotension [MedDRA:10021097]
Arterial hypotension [MedDRA:10021097]
Quality:
Cross references:
Orphanet:35240 "Hypotension" [Orphanet:35240]
OMIM: "Arterial hypotension" [OMIM:Arterial hypotension]
OMIM: "Hypotension" [OMIM:Hypotension]
OMIM: "Low blood pressure" [OMIM:Low blood pressure]
UMLS:C0020649 "Hypotension" [HPO:0002615]
UMLS:C0020649 "Hypotension" [Orphanet:35240]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
MedDRA Vascular tests NEC (incl blood pressure)
MedDRA Vascular hypotensive disorders
HPO         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)
             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)
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)