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newborn respiratory distress syndrome
Summary
- Synonym
-
- HMD - Hyaline membrane disease
- Neonatal respiratory Distress syndrome
- hyaline membrane disease
- pulmonary hyaline membrane disease
- pulmonary hypoperfusion syndrome of newborn
- respiratory distress syndrome of newborn
- Definition
- A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts.
- Super Class
- respiratory failure
External Links
- Disease Ontology
- DOID:12716
- Mondo Disease Ontology
- MeSH
- UMLS
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5291 | PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | |
| 5293 | PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | |
| 5294 | PIK3CG | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | |
| 5319 | PLA2G1B | phospholipase A2 group IB | |
| 5320 | PLA2G2A | phospholipase A2 group IIA | |
| 5321 | PLA2G4A | phospholipase A2 group IVA | |
| 5329 | PLAUR | plasminogen activator, urokinase receptor | |
| 5337 | PLD1 | phospholipase D1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P17405 | Sphingomyelin phosphodiesterase | |
| P17931 | Galectin-3 | |
| P19835 | Bile salt-activated lipase | |
| P20815 | Cytochrome P450 3A5 | |
| P21589 | 5'-nucleotidase | |
| P22309 | UDP-glucuronosyltransferase 1A1 | |
| P34913 | Bifunctional epoxide hydrolase 2 | |
| P35247 | Pulmonary surfactant-associated protein D | |
| P35354 | Prostaglandin G/H synthase 2 | |
| P40925 | Malate dehydrogenase, cytoplasmic |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002615 | Hypotension |
| HP:0001649 | Tachycardia |
| HP:0012418 | Hypoxemia |
| HP:0000961 | Cyanosis |
| HP:0002878 | Respiratory failure |
| HP:0100750 | Atelectasis |
| HP:0001695 | Cardiac arrest |
| HP:0000765 | Abnormal thorax morphology |
| HP:0002789 | Tachypnea |
| HP:0100598 | Pulmonary edema |
