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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

MONDO:0009971

MeSH

D006819

UMLS

C0020192

OMIM

267450

MGI genotype (from TogoID)

Related Genes

Displaying entries **31 - 40** of 70 in total

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Gene ID	Gene Symbol	Description	Source
5048	PAFAH1B1	platelet activating factor acetylhydrolase 1b regulatory subunit 1	DisGeNET
5290	PIK3CA	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	DisGeNET
5291	PIK3CB	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta	DisGeNET
5293	PIK3CD	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	DisGeNET
5294	PIK3CG	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	DisGeNET
5319	PLA2G1B	phospholipase A2 group IB	DisGeNET
5320	PLA2G2A	phospholipase A2 group IIA	DisGeNET DisGeNET
5321	PLA2G4A	phospholipase A2 group IVA	DisGeNET
5329	PLAUR	plasminogen activator, urokinase receptor	DisGeNET
5337	PLD1	phospholipase D1	DisGeNET

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
15531	Ndst1	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
29633	Ndst1	N-deacetylase and N-sulfotransferase 1	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
38736	sfl	sulfateless	Alliance of Genome Resources

Displaying **all 2** entries
Gene ID	Gene Symbol	Description	Source
570459	ndst1b	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b	Alliance of Genome Resources
100329944	ndst1a	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1a	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source	Organism
496577	ndst1	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Alliance of Genome Resources	Xenopus tropicalis (tropical clawed frog)

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
177675	hst-1	Heparan sulfate N-sulfotransferase 1	Alliance of Genome Resources

Related Glycoprotein

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UniProt ID	Protein Name	Source
P40939	Trifunctional enzyme subunit alpha, mitochondrial	DisGeNET
P42338	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform	DisGeNET
P42765	3-ketoacyl-CoA thiolase, mitochondrial	DisGeNET
P43034	Platelet-activating factor acetylhydrolase IB subunit beta	DisGeNET
P43490	Nicotinamide phosphoribosyltransferase	DisGeNET
P47712	Cytosolic phospholipase A2	DisGeNET
P48736	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform	DisGeNET
P49419	Alpha-aminoadipic semialdehyde dehydrogenase	DisGeNET
P51606	N-acylglucosamine 2-epimerase	DisGeNET
P51689	Arylsulfatase D	DisGeNET DisGeNET

The Human Phenotype Ontology

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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