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Details
Link-It Detail - Disease - Learning Disabilities
Debug Stats
  • ### Total Build Time: 41 ms 25.235 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 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=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 23.574 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Learning Disabilities C0751265
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBBS12166379Bardet-Biedl syndrome 12
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanBBS5129880Bardet-Biedl syndrome 5
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanTTC8123016tetratricopeptide repeat domain 8
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanTMEM6791147transmembrane protein 67
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanARL684100ADP-ribosylation factor-like 6
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanBBS1079738Bardet-Biedl syndrome 10
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanADCK356997aarF domain containing kinase 3
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanBBS755212Bardet-Biedl syndrome 7
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanAPTX54840aprataxin
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanBBS927241Bardet-Biedl syndrome 9
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanPDSS123590prenyl (decaprenyl) diphosphate synthase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanTRIM3222954tripartite motif containing 32
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanIL1RAPL111141interleukin 1 receptor accessory protein-like 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanMKKS8195McKusick-Kaufman syndrome
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanTBX16899T-box 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
HumanNF14763neurofibromin 1
img OMIM, Score=1000, UMLKSK CUI: C0751265
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751265Learning Disabilities0self