Neonatal respiratory distress
Symptom Information:
Symptom ID: | HPO:0002643 | |||||||
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) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Neonatal respiratory distress(HPO:0002643) Functional respiratory abnormality(HPO:0002795) Respiratory insufficiency(HPO:0002093) Neonatal respiratory distress(HPO:0002643) MedDRA: |
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Database Frequency: | 22 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
3M syndrome | (Orphanet:2616) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Brain-lung-thyroid syndrome | (Orphanet:209905) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Cleidocranial dysplasia | (Orphanet:1452) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Fetal Gaucher disease | (Orphanet:85212) |
Hyper-beta-alaninemia | (Orphanet:309147) |
Infant acute respiratory distress syndrome | (Orphanet:70587) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Isolated Pierre Robin syndrome | (Orphanet:718) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Steinert myotonic dystrophy | (Orphanet:273) |
THORACOPELVIC DYSOSTOSIS | (OMIM:187770) |
THREE M SYNDROME 1 | (OMIM:273750) |
X-linked centronuclear myopathy | (Orphanet:596) |