Tachypnea
Symptom Information:
Symptom ID: | HPO:0002789 | ||||
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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Abnormal pattern of respiration(HPO:0002793) Tachypnea(HPO:0002789) MedDRA: |
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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) |