Respiratory distress

Symptom Information:

Symptom ID: HPO:0002098
Synonyms:
Respiratory distress (finding) [Orphanet:33100]
Respiratory distress [Orphanet:33100]
Respiratory distress [OMIM:Respiratory distress]
Respiratory distress/dyspnea/respiratory failure/lung volume reduction [Orphanet:33100]
Respiratory distress [MedDRA:10038687]
Distress respiratory [MedDRA:10038687]
Respiratory distress (congenital form) [OMIM:Respiratory distress (congenital form)]
Respiratory distress (in 1 patient) [OMIM:Respiratory distress (in 1 patient)]
Respiratory distress (in some patients) [OMIM:Respiratory distress (in some patients)]
Respiratory distress (neonate) [OMIM:Respiratory distress (neonate)]
Lung volume reduction [Orphanet:33100]
Quality:
Cross references:
Orphanet:33100 "Respiratory distress/dyspnea/respiratory failure/lung volume reduction" [Orphanet:33100]
OMIM: "Respiratory distress" [OMIM:Respiratory distress]
OMIM: "Respiratory distress (congenital form)" [OMIM:Respiratory distress (congenital form)]
OMIM: "Respiratory distress (in 1 patient)" [OMIM:Respiratory distress (in 1 patient)]
OMIM: "Respiratory distress (in some patients)" [OMIM:Respiratory distress (in some patients)]
OMIM: "Respiratory distress (neonate)" [OMIM:Respiratory distress (neonate)]
UMLS:C0476273 "Respiratory distress" [Orphanet:33100]
Is a (Direct Parents):
Orphanet Respiratory insufficiency
MedDRA Breathing abnormalities
Orphanet Abnormality of the respiratory system
HPO         Dyspnea
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)
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)