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Details
Link-It Detail - Disease - Chiari malformation type II
Debug Stats
  • ### Total Build Time: 97 ms 18.607 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 352 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=73 ms Completed: 73 ms rowSize= 12.338 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 4.694 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Chiari malformation type II C0555206
Relationships (26)

Relation Types:
diso_​to_​diso : 26


Relationships:
alias_​of : 1
inheritance_​type_​of : 1
manifestation_​of : 24
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Absent cisterna magna C2673902
DISO_to_DISOmanifestation_ofimg Associated with syringomyelia (186700) C2673908
DISO_to_DISOmanifestation_ofimg Ataxia C0004134
DISO_to_DISOmanifestation_ofimg Bulbar signs C1856507
DISO_to_DISOmanifestation_ofimg CERVICAL MYELOPATHY C0149645
DISO_to_DISOalias_ofimg Chiari malformation type II C0555206
DISO_to_DISOmanifestation_ofimg Choking C0008301
DISO_to_DISOmanifestation_ofimg Choristoma C0008519
DISO_to_DISOmanifestation_ofimg Deglutition Disorders C0011168
DISO_to_DISOmanifestation_ofimg Feeding poor C0576456
DISO_to_DISOmanifestation_ofimg HEADACHE, OCCIPITAL C0231613
DISO_to_DISOmanifestation_ofimg Herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum C2673900
DISO_to_DISOmanifestation_ofimg Hydrocephalus C0020255
DISO_to_DISOinheritance_type_ofimg Multifactorial C1837655
DISO_to_DISOmanifestation_ofimg Muscle Hypotonia C0026827
DISO_to_DISOmanifestation_ofimg Muscle Spasticity C0026838
DISO_to_DISOmanifestation_ofimg Nystagmus C0028738
DISO_to_DISOmanifestation_ofimg Open spina bifida (myelomeningocele, 182940) C2673907
DISO_to_DISOmanifestation_ofimg Opisthotonus C0151818
DISO_to_DISOmanifestation_ofimg Partial or total agenesis of the corpus callosum (33%) C2673905
DISO_to_DISOmanifestation_ofimg Polygyria C2673903
DISO_to_DISOmanifestation_ofimg Small, thin cerebellum C2673901
DISO_to_DISOmanifestation_ofimg Subnormal intelligence (62%) C2673906
DISO_to_DISOmanifestation_ofimg Symptom onset at birth or infancy Arnold-Chiari type II is uniquely associated with myelomeninogocele (182940) C2673910
DISO_to_DISOmanifestation_ofimg Upper limb weakness C2678063
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0555206
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0555206
HumanPOR5447P450 (cytochrome) oxidoreductase
img OMIM, Score=1000, UMLKSK CUI: C0555206
HumanFGFR22263fibroblast growth factor receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0555206
HumanFGFR12260fibroblast growth factor receptor 1
img OMIM, Score=1000, UMLKSK CUI: C0555206
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0555206Chiari malformation type II0self