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Details
Link-It Detail - Disease - DETERIORATION MENTAL (NOS)
Debug Stats
  • ### Total Build Time: 53 ms 16.927 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 350 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=4 ms Completed: 4 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 15.251 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
DETERIORATION MENTAL (NOS) C0234985
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanNHLRC1378884NHL repeat containing 1
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanAPTX54840aprataxin
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanNPC210577Niemann-Pick disease, type C2
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanITM2B9445integral membrane protein 2B
img OMIM, Score=882, UMLKSK CUI: C0234985
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanXPA7507xeroderma pigmentosum, complementation group A
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanSCN1A6323sodium channel, voltage-gated, type I, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanNPC14864Niemann-Pick disease, type C1
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanGALC2581galactosylceramidase
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanGABRG22566gamma-aminobutyric acid (GABA) A receptor, gamma 2
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanERCC22068excision repair cross-complementing rodent repair deficiency, complementation group 2
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanCLN82055ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanTIMM8A1678translocase of inner mitochondrial membrane 8 homolog A (yeast)
img OMIM, Score=1000, UMLKSK CUI: C0234985
HumanCLN51203ceroid-lipofuscinosis, neuronal 5
img GENERIF, Score=1000, Pubmed Id: 17607606, UMLKSK CUI: C0234985
HumanARSA410arylsulfatase A
img OMIM, Score=1000, UMLKSK CUI: C0234985
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0234985DETERIORATION MENTAL (NOS)0self