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Details
Link-It Detail - Disease - FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
Debug Stats
  • ### Total Build Time: 32 ms 27.559 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 386 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=24 ms Completed: 24 ms rowSize= 12.104 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 13.829 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED C1833296
Relationships (37)

Relation Types:
diso_​to_​diso : 37


Relationships:
alias_​of : 1
manifestation_​of : 36
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Aggression C0001807
DISO_to_DISOmanifestation_ofimg Agitation C0085631
DISO_to_DISOmanifestation_ofimg Astrocytosis C0751171
DISO_to_DISOmanifestation_ofimg Average age of onset 57 years C1833304
DISO_to_DISOmanifestation_ofimg Average duration of illness 8 years C1833305
DISO_to_DISOmanifestation_ofimg Babinski Reflex C0034935
DISO_to_DISOmanifestation_ofimg Caused by mutation in the chromatin-modifying protein 2B (CHMP2B, 609512.0001) C1833303
DISO_to_DISOmanifestation_ofimg Change in personality C0240735
DISO_to_DISOmanifestation_ofimg Cognitive decline, progressive C1863063
DISO_to_DISOmanifestation_ofimg Cortical neuronal loss C1833299
DISO_to_DISOmanifestation_ofimg Disorder characterised by myoclonus C0027066
DISO_to_DISOmanifestation_ofimg Dyscalculia C0869474
DISO_to_DISOmanifestation_ofimg Dystonia C0013421
DISO_to_DISOalias_ofimg FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED C1833296
DISO_to_DISOmanifestation_ofimg Frontal release reflexes C1833297
DISO_to_DISOmanifestation_ofimg Frontotemporal Dementia C0338451
DISO_to_DISOmanifestation_ofimg Gait abnormality C0575081
DISO_to_DISOmanifestation_ofimg Generalized cortical atrophy, most prominent in the frontal and parietal lobes C1833298
DISO_to_DISOmanifestation_ofimg Global reduction in cerebral blood flow on PET scan C1833301
DISO_to_DISOmanifestation_ofimg Hyperorality C1843802
DISO_to_DISOmanifestation_ofimg Hyperreflexia C0151889
DISO_to_DISOmanifestation_ofimg Inappropriate behavior C0233522
DISO_to_DISOmanifestation_ofimg Indifferent mood C0085632
DISO_to_DISOmanifestation_ofimg Lack of insight C0233824
DISO_to_DISOmanifestation_ofimg Lingual-Facial-Buccal Dyskinesia C0152115
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanSLC40A130061solute carrier family 40 (iron-regulated transporter), member 1
img GENERIF, Score=1000, Pubmed Id: 14768003, UMLKSK CUI: C1833296
HumanUBE2D17321ubiquitin-conjugating enzyme E2D 1
img GENERIF, Score=694, Pubmed Id: 15139022, UMLKSK CUI: C1833296
HumanTFRC7037transferrin receptor (p90, CD71)
img GENERIF, Score=1000, Pubmed Id: 15880641, UMLKSK CUI: C1833296
HumanSLC11A24891solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
img GENERIF, Score=1000, Pubmed Id: 14768003, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 15880641, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 12734107, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 12209011, UMLKSK CUI: C1833296
img GENERIF, Score=694, Pubmed Id: 15139022, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 18419598, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 18667808, UMLKSK CUI: C1833296
img GENERIF, Score=694, Pubmed Id: 16123094, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 12127992, UMLKSK CUI: C1833296
img GENERIF, Score=694, Pubmed Id: 16439678, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 15459009, UMLKSK CUI: C1833296
img GENERIF, Score=1000, Pubmed Id: 17109629, UMLKSK CUI: C1833296
img GENERIF, Score=827, Pubmed Id: 15024413, UMLKSK CUI: C1833296
HumanHFE3077hemochromatosis
img GENERIF, Score=1000, Pubmed Id: 15880641, UMLKSK CUI: C1833296
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1833296FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED0self