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Details
Link-It Detail - Disease - Low Birth Weights
Debug Stats
  • ### Total Build Time: 79 ms 31.411 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 289 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 2.544 KB
  • CONCEPT_GENES gt=44 ms Completed: 44 ms rowSize= 27.039 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Low Birth Weights C0024032
Definition (1)
Refers to a fetus or infant who is smaller than expected for the age or gender, or who has a birthweight less than the 10th percentile.
Relationships (4)

Relation Types:
diso_​to_​diso : 4


Relationships:
isa : 1
mapped_​to : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg INFANT VLBW C0282667
DISO_to_DISOmapped_toimg Interuterine growth retard C0541995
DISO_to_DISOpermuted_term_ofimg Low Birth Weights C0024032
DISO_to_DISOmapped_toimg Small for gestational age (disorder) C0235991
Genes (42)

Species:
human : 42
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanMCPH179648microcephalin 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanTLR954106toll-like receptor 9
img GENERIF, Score=1000, Pubmed Id: 16779724, UMLKSK CUI: C0024032
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanLGALS1329124lectin, galactoside-binding, soluble, 13
img GENERIF, Score=1000, Pubmed Id: 18186153, UMLKSK CUI: C0024032
HumanCUL79820cullin 7
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanFZD48322frizzled family receptor 4
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanPHLDA27262pleckstrin homology-like domain, family A, member 2
img GENERIF, Score=1000, Pubmed Id: 17180344, UMLKSK CUI: C0024032
HumanTSHR7253thyroid stimulating hormone receptor
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 12496175, UMLKSK CUI: C0024032
HumanTHRB7068thyroid hormone receptor, beta
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanPPARG5468peroxisome proliferator-activated receptor gamma
img GENERIF, Score=1000, Pubmed Id: 15201543, UMLKSK CUI: C0024032
img GENERIF, Score=1000, Pubmed Id: 19000312, UMLKSK CUI: C0024032
HumanPIK3CG5294phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
img GENERIF, Score=1000, Pubmed Id: 19011679, UMLKSK CUI: C0024032
HumanPDHA15160pyruvate dehydrogenase (lipoamide) alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanSERPINE15054serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
img GENERIF, Score=679, Pubmed Id: 11809921, UMLKSK CUI: C0024032
img GENERIF, Score=1000, Pubmed Id: 17555513, UMLKSK CUI: C0024032
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanMYH34621myosin, heavy chain 3, skeletal muscle, embryonic
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanMEST4232mesoderm specific transcript
img GENERIF, Score=1000, Pubmed Id: 17450433, UMLKSK CUI: C0024032
HumanKCNJ113767potassium inwardly-rectifying channel, subfamily J, member 11
img OMIM, Score=1000, UMLKSK CUI: C0024032
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0024032
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0024032Low Birth Weights0self