Respiratory distress
Symptom Information:
Symptom ID: | HPO:0002098 | |||||||||||
Synonyms: |
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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) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) Respiratory distress(HPO:0002098) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) Respiratory distress(HPO:0002098) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory disorders NEC(MedDRA:10038716) Breathing abnormalities(MedDRA:10006334) Respiratory distress(HPO:0002098) |
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Database Frequency: | 75 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Alström syndrome | (Orphanet:64) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Atrial tachyarrhythmia with short PR interval | (Orphanet:844) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Brain-lung-thyroid syndrome | (Orphanet:209905) |
CAMPOMELIC DYSPLASIA | (OMIM:114290) |
CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 | (OMIM:615595) |
Campomelic dysplasia | (Orphanet:140) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Chronic respiratory distress with surfactant metabolism deficiency | (Orphanet:217566) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital laryngeal web | (Orphanet:2374) |
Congenital laryngomalacia | (Orphanet:2373) |
Congenital lobar emphysema | (Orphanet:1928) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
DPM1-CDG | (Orphanet:79322) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Diabetic embryopathy | (Orphanet:1926) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Fetal Gaucher disease | (Orphanet:85212) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Goldblatt syndrome | (Orphanet:166272) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Incessant infant ventricular tachycardia | (Orphanet:45453) |
Kniest dysplasia | (Orphanet:485) |
Left ventricular noncompaction 10 | (OMIM:615396) |
Leigh syndrome | (Orphanet:506) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 | (OMIM:616268) |
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY | (OMIM:614741) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
Maple syrup urine disease | (Orphanet:511) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multifocal atrial tachycardia | (Orphanet:3282) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Neonatal acute respiratory distress with surfactant metabolism deficiency | (Orphanet:217563) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 9 | (OMIM:613824) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Pyruvate carboxylase deficiency | (Orphanet:3008) |
Reticular dysgenesis | (Orphanet:33355) |
SUCCINIC ACIDEMIA | (OMIM:600335) |
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3 | (OMIM:610921) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Steinert myotonic dystrophy | (Orphanet:273) |
Sterile multifocal osteomyelitis with periostitis and pustulosis | (Orphanet:210115) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Wolfram syndrome | (Orphanet:3463) |