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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 |
|---|---|---|---|
| 8398 | PLA2G6 | phospholipase A2 group VI | |
| 8399 | PLA2G10 | phospholipase A2 group X | |
| 8818 | DPM2 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | |
| 9365 | KL | klotho | |
| 9468 | PCYT1B | phosphate cytidylyltransferase 1B, choline | |
| 10135 | NAMPT | nicotinamide phosphoribosyltransferase | |
| 10449 | ACAA2 | acetyl-CoA acyltransferase 2 | |
| 10998 | SLC27A5 | solute carrier family 27 member 5 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 27163 | NAAA | N-acylethanolamine acid amidase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8IWL1 | Pulmonary surfactant-associated protein A2 | |
| Q8IWL2 | Pulmonary surfactant-associated protein A1 | |
| Q8NF37 | Lysophosphatidylcholine acyltransferase 1 | |
| Q99798 | Aconitate hydratase, mitochondrial | |
| Q9P126 | C-type lectin domain family 1 member B | |
| Q9UEF7 | Klotho |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001662 | Bradycardia |
| HP:0100806 | Sepsis |
| HP:0002090 | Pneumonia |
| HP:0001622 | Premature birth |
| HP:0011947 | Respiratory tract infection |
