ONTOLOGY REPORT - ANNOTATIONS


Term:newborn respiratory distress syndrome
go back to main search page
Accession:DOID:12716 term browser browse the term
Definition:A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause.
Synonyms:exact_synonym: HMD - Hyaline membrane disease;   Neonatal Respiratory Distress Syndrome;   infantile respiratory distress syndrome;   pulmonary hyaline membrane disease;   pulmonary hypoperfusion syndrome of newborn;   respiratory distress syndrome of newborn;   respiratory distress syndrome, infant
 primary_id: MESH:D012127
 alt_id: OMIA:000101;   RDO:0002596
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
newborn respiratory distress syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cat catalase JBrowse link 3 93,379,872 93,412,058 RGD:8655661
G Epas1 endothelial PAS domain protein 1 JBrowse link 6 10,306,508 10,385,239 RGD:13592920
G Hmox1 heme oxygenase 1 JBrowse link 19 14,508,634 14,515,455 RGD:4145353
G Icam1 intercellular adhesion molecule 1 JBrowse link 8 22,035,287 22,047,049 RGD:4145440
RGD:4145493
G Mbl2 mannose binding lectin 2 JBrowse link 1 248,435,069 248,442,669 RGD:12910849
G Megf10 multiple EGF-like domains 10 JBrowse link 18 52,215,652 52,366,212 RGD:11554173
G Mif macrophage migration inhibitory factor JBrowse link 20 13,715,219 13,732,980 RGD:4891007
G Ndst1 N-deacetylase and N-sulfotransferase 1 JBrowse link 18 55,951,497 56,014,107 RGD:13592920
G Npsr1 neuropeptide S receptor 1 JBrowse link 8 25,246,174 25,483,582 RGD:4891932
G Sftpa1 surfactant protein A1 JBrowse link 16 18,716,019 18,719,404 RGD:4143433
RGD:4143428
G Sftpb surfactant protein B JBrowse link 4 100,166,855 100,175,941 RGD:4143416
RGD:4143455
RGD:4143433
RGD:4143428
RGD:4143418
RGD:4143376
G Sftpc surfactant protein C JBrowse link 15 52,211,538 52,214,480 RGD:4143428
RGD:4144127
G Sftpd surfactant protein D JBrowse link 16 18,753,535 18,766,100 RGD:4143507
RGD:4143428
G Sod1 superoxide dismutase 1 JBrowse link 11 30,363,282 30,368,858 RGD:8655661
G Tnnt2 troponin T2, cardiac type JBrowse link 13 52,662,974 52,680,992 RGD:11554173
G Vegfa vascular endothelial growth factor A JBrowse link 9 17,340,341 17,355,681 RGD:13592920
autosomal recessive distal spinal muscular atrophy 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ighmbp2 immunoglobulin mu DNA binding protein 2 JBrowse link 1 218,509,274 218,531,922 RGD:737748
RGD:8554872
RGD:7240710
G Spg7 SPG7 matrix AAA peptidase subunit, paraplegin JBrowse link 19 55,880,549 55,914,729 RGD:8554872
Brain-Lung-Thyroid Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nkx2-1 NK2 homeobox 1 JBrowse link 6 77,418,096 77,423,383 RGD:7240710
RGD:8554872
RGD:12914768
RGD:12914769
RGD:11073166
RGD:12914770
CHITAYAT SYNDROME term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Erf Ets2 repressor factor JBrowse link 1 82,112,449 82,120,902 RGD:8554872
RGD:7240710
Hyaline Membrane Disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Serpine1 serpin family E member 1 JBrowse link 12 22,641,104 22,651,482 RGD:4144850
G Sftpc surfactant protein C JBrowse link 15 52,211,538 52,214,480 RGD:4143444
Kniest dysplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:7240710
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      respiratory system disease 2375
        lung disease 1370
          newborn respiratory distress syndrome 22
            Brain-Lung-Thyroid Syndrome 1
            CHITAYAT SYNDROME 1
            Hyaline Membrane Disease + 3
            RDS - Infants 0
            Transient Tachypnea of the Newborn 0
            autosomal recessive distal spinal muscular atrophy 1 2
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      respiratory system disease 2375
        lower respiratory tract disease 1412
          lung disease 1370
            respiratory failure 176
              newborn respiratory distress syndrome 22
                Brain-Lung-Thyroid Syndrome 1
                CHITAYAT SYNDROME 1
                Hyaline Membrane Disease + 3
                RDS - Infants 0
                Transient Tachypnea of the Newborn 0
                autosomal recessive distal spinal muscular atrophy 1 2
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.