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Details
Link-It Detail - Disease - Hyaline Membrane Disease
Debug Stats
  • ### Total Build Time: 96 ms 14.450 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 468 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=13 ms Completed: 13 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=27 ms Completed: 27 ms rowSize= 4.161 KB
  • CONCEPT_RELATIONSHIPS gt=39 ms Completed: 39 ms rowSize= 5.957 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 1.597 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyaline Membrane Disease C0020192
Definition (1)
A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS).
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Respiratory Distress Syndrome, Newborn C0035220
Ancestral Roots
RootRoot Plus OneDepthParent
img Respiratory Tract Diseases C0035242img Lung Diseases C00241154img Respiratory Distress Syndrome, Newborn C0035220
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212905img Respiratory Distress Syndrome, Newborn C0035220
img Respiratory Tract Diseases C0035242img Respiration Disorders C00352044img Respiratory Distress Syndrome, Newborn C0035220
Relationships (11)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 1
diso_​to_​diso : 8


Relationships:
none : 3
associated_​with : 2
location_​of : 1
mapped_​to : 3
permuted_​term_​of : 1
replaces : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM6img Pulmonary Surfactants C0034085
DISO_to_ANAT4img Lung C0024109
DISO_to_DISO4img Complication Aspects C1171258
DISO_to_ANATlocation_ofimg Structure of terminal bronchiole C0225666
DISO_to_DISOmapped_toimg Arthrosis, flat face, hypotonia, short neck and macrocephaly C1855605
DISO_to_DISOpermuted_term_ofimg Hyaline Membrane Disease C0020192
DISO_to_DISOassociated_withimg Hyaline membrane C0333563
DISO_to_DISOmapped_toimg KNIEST DYSPLASIA C0265279
DISO_to_DISOassociated_withimg Newborn, premature birth C0233315
DISO_to_DISOmapped_toimg Rambaud Galian syndrome C2930864
DISO_to_DISOreplacesimg Respiratory Distress Syndrome, Newborn C0035220
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanNFKB14790nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
img GENERIF, Score=1000, Pubmed Id: 15746262, UMLKSK CUI: C0020192
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020192Hyaline Membrane Disease0self