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 61 - 70 of 70 in total
Gene ID Gene Symbol Description Source
27306 HPGDS hematopoietic prostaglandin D synthase
51266 CLEC1B C-type lectin domain family 1 member B
54658 UGT1A1 UDP glucuronosyltransferase family 1 member A1
57016 AKR1B10 aldo-keto reductase family 1 member B10
79888 LPCAT1 lysophosphatidylcholine acyltransferase 1
81031 SLC2A10 solute carrier family 2 member 10
83666 PARP9 poly(ADP-ribose) polymerase family member 9
151056 PLB1 phospholipase B1
653509 SFTPA1 surfactant protein A1
729238 SFTPA2 surfactant protein A2
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