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Details
Link-It Detail - Disease - ARCL1
Debug Stats
  • ### Total Build Time: 149 ms 15.637 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 308 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=128 ms Completed: 128 ms rowSize= 12.487 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 1.639 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.140 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
ARCL1 C0268351
Relationships (28)

Relation Types:
diso_​to_​diso : 26
diso_​to_​phys : 2


Relationships:
expanded_​form_​of : 1
isa : 2
manifestation_​of : 25
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOexpanded_form_ofimg ARCL1 C0268351
DISO_to_DISOmanifestation_ofimg Aneurysm of ascending aorta C0856747
DISO_to_DISOmanifestation_ofimg Aortic Stenosis, Supravalvular C0003499
DISO_to_DISOmanifestation_ofimg BLADDER DIVERTICULUM C0156273
DISO_to_DISOmanifestation_ofimg Caused by mutation in the EGF-containing fibulin-like extracellular matrix protein 2 gene (EFEMP2, 604633.0001) C2673777
DISO_to_DISOmanifestation_ofimg Caused by mutation in the fibulin 5 gene (FBLN5, 604580.0001) C2673778
DISO_to_DISOmanifestation_ofimg Congenital funnel chest C0016842
DISO_to_DISOmanifestation_ofimg Cutis Laxa C0010495
DISO_to_DISOisaimg Cutis laxa, recessive, type I C0432336
DISO_to_DISOisaimg Cutis laxa, recessive, type II C0432337
DISO_to_DISOmanifestation_ofimg Diaphragmatic Hernia C0019284
DISO_to_DISOmanifestation_ofimg Excessive skin folds C2673772
DISO_to_DISOmanifestation_ofimg HERNIA, INGUINAL C0019294
DISO_to_DISOmanifestation_ofimg Hernia, Diaphragmatic C0019284
DISO_to_DISOmanifestation_ofimg Hernia, Inguinal C0019294
DISO_to_DISOmanifestation_ofimg Increased vascularization, reduced collagen bundle size C2673774
DISO_to_DISOmanifestation_ofimg Loose redundant skin C1844692
DISO_to_DISOmanifestation_ofimg No skin hyperelasticity C2673773
DISO_to_DISOmanifestation_ofimg Normal wound healing C1863751
DISO_to_DISOmanifestation_ofimg Oligohydramnios C0079924
DISO_to_DISOmanifestation_ofimg Pulmonary Emphysema C0034067
DISO_to_DISOmanifestation_ofimg Recurrent respiratory infections C1866203
DISO_to_DISOmanifestation_ofimg Sagging cheeks C2673771
DISO_to_DISOmanifestation_ofimg Umbilical hernia C0019322
DISO_to_DISOmanifestation_ofimg Underdeveloped elastic fibers in dermis C2673775
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
img GENERIF, Score=734, Pubmed Id: 18157129, UMLKSK CUI: C0268351
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268351ARCL10self