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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 |
|---|---|---|---|
| 1543 | CYP1A1 | cytochrome P450 family 1 subfamily A member 1 | |
| 1544 | CYP1A2 | cytochrome P450 family 1 subfamily A member 2 | |
| 1545 | CYP1B1 | cytochrome P450 family 1 subfamily B member 1 | |
| 1551 | CYP3A7 | cytochrome P450 family 3 subfamily A member 7 | |
| 1577 | CYP3A5 | cytochrome P450 family 3 subfamily A member 5 | |
| 1634 | DCN | decorin | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 2053 | EPHX2 | epoxide hydrolase 2 | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 3030 | HADHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha |
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 |
