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Details
Link-It Detail - Disease - Hypoventilation
Debug Stats
  • ### Total Build Time: 56 ms 11.412 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 240 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 1,010 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 570 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=13 ms Completed: 13 ms rowSize= 2.824 KB
  • CONCEPT_RELATIONSHIPS gt=3 ms Completed: 3 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 4.997 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypoventilation C0398353
Definition (1)
A reduction in the amount of air entering the pulmonary alveoli.
Semantic Types (2)
Pathologic Function (T046)
Sign or Symptom (T184)
Parents (2)
img Respiratory Insufficiency C0035229
img Signs and Symptoms, Respiratory C0037090
Children (1)
img Obesity Hypoventilation Syndrome C0031880
Ancestral Roots
RootRoot Plus OneDepthParent
img Respiratory Tract Diseases C0035242img Respiration Disorders C00352044img Respiratory Insufficiency C0035229
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Signs and Symptoms, Respiratory C0037090
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanMOGS7841mannosyl-oligosaccharide glucosidase
img OMIM, Score=1000, UMLKSK CUI: C0398353
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0398353
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C0398353
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img OMIM, Score=833, UMLKSK CUI: C0398353
HumanHOXA13198homeobox A1
img GENERIF, Score=1000, Pubmed Id: 16155570, UMLKSK CUI: C0398353
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0398353Hypoventilation0self