Tachypnea

Symptom Information:

Symptom ID: HPO:0002789
Synonyms:
Increased respiratory rate or depth of breathing [HPO:0002789]
Polypnea [HPO:0002789]
Polypnea [OMIM:Polypnea]
Tachypnea [OMIM:Tachypnea]
Quality:
Cross references:
OMIM: "Polypnea" [OMIM:Polypnea]
OMIM: "Tachypnea" [OMIM:Tachypnea]
UMLS:C1142291 "Polypnea" [HPO:0002789]
Is a (Direct Parents):
HPO         Abnormal pattern of respiration
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Functional respiratory abnormality(HPO:0002795)
             Abnormal pattern of respiration(HPO:0002793)
                Tachypnea(HPO:0002789)
MedDRA:
Database Frequency: 48 / 7739
Resource:

All diseases associated with this symptom:

Argininosuccinic aciduria (Orphanet:23)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Biotinidase deficiency (Orphanet:79241)
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO (OMIM:615751)
CHOLESTEROL PNEUMONIA (OMIM:215030)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Chronic respiratory distress with surfactant metabolism deficiency (Orphanet:217566)
Citrullinemia type I (Orphanet:247525)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Cryptogenic organizing pneumonia (Orphanet:1302)
Desquamative interstitial pneumonia (Orphanet:98852)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial isolated restrictive cardiomyopathy (Orphanet:75249)
His bundle tachycardia (Orphanet:3283)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (Orphanet:401948)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Infant acute respiratory distress syndrome (Orphanet:70587)
Infantile hypophosphatasia (Orphanet:247651)
Joubert syndrome 21 (OMIM:615636)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Lymphoid interstitial pneumonia (Orphanet:79128)
METHIONINE MALABSORPTION SYNDROME (OMIM:250900)
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME (OMIM:613834)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Multifocal atrial tachycardia (Orphanet:3282)
Neonatal acute respiratory distress with surfactant metabolism deficiency (Orphanet:217563)
Neonatal hemochromatosis (Orphanet:446)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Ornithine transcarbamylase deficiency (Orphanet:664)
Propionic acidemia (Orphanet:35)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Pyruvate carboxylase deficiency (Orphanet:3008)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Pyruvate dehydrogenase phosphatase deficiency (Orphanet:79246)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 (OMIM:265120)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3 (OMIM:610921)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4 (OMIM:300770)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Succinyl-CoA:3-ketoacid CoA transferase deficiency (Orphanet:832)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)