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
Displaying entries 51 - 60 of 70 in total
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
15531 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
29633 Ndst1 N-deacetylase and N-sulfotransferase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
38736 sfl sulfateless
Displaying all 2 entries
Gene ID Gene Symbol Description Source
570459 ndst1b N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b
100329944 ndst1a N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1a
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
496577 ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
177675 hst-1 Heparan sulfate N-sulfotransferase 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 15 in total
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
Displaying 1 entry
Gene ID Gene Symbol Description
6440 SFTPC surfactant protein C

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024