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Details
Link-It Detail - Disease - Mild Mental Retardation
Debug Stats
  • ### Total Build Time: 21 ms 17.887 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 344 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=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=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 16.220 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Mild Mental Retardation C0026106
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanPHF684295PHD finger protein 6
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanCDKL351265cyclin-dependent kinase-like 3
img GENERIF, Score=861, Pubmed Id: 18412109, UMLKSK CUI: C0026106
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanMLC123209megalencephalic leukoencephalopathy with subcortical cysts 1
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanOPHN14983oligophrenin 1
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanMYF64618myogenic factor 6 (herculin)
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanMSH24436mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
img OMIM, Score=909, UMLKSK CUI: C0026106
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanFMR12332fragile X mental retardation 1
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanFLNA2316filamin A, alpha
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanEYA12138eyes absent homolog 1 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanDNMT3B1789DNA (cytosine-5-)-methyltransferase 3 beta
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanDMD1756dystrophin
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanBLM641Bloom syndrome, RecQ helicase-like
img OMIM, Score=1000, UMLKSK CUI: C0026106
HumanJAG1182jagged 1
img OMIM, Score=1000, UMLKSK CUI: C0026106
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0026106Mild Mental Retardation0self