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Details
Link-It Detail - Disease - Cerebral Amyloid Angiopathy, Familial
Debug Stats
  • ### Total Build Time: 67 ms 20.622 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 286 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=9 ms Completed: 9 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.420 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=44 ms Completed: 44 ms rowSize= 11.927 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 5.199 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cerebral Amyloid Angiopathy, Familial C0268393
Definition (1)
A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Amyloidosis, Familial C0740340
img Brain Diseases, Metabolic, Inborn C0752109
img Cerebral Amyloid Angiopathy C0085220
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501235img Amyloidosis, Familial C0740340
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255175img Amyloidosis, Familial C0740340
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255176img Amyloidosis, Familial C0740340
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501235img Brain Diseases, Metabolic, Inborn C0752109
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255175img Brain Diseases, Metabolic, Inborn C0752109
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076826img Brain Diseases, Metabolic, Inborn C0752109
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255176img Cerebral Amyloid Angiopathy C0085220
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076828img Cerebral Amyloid Angiopathy C0085220
img Cardiovascular Diseases C0007222img Vascular Diseases C00423737img Cerebral Amyloid Angiopathy C0085220
Relationships (10)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 2
diso_​to_​diso : 5
diso_​to_​phen : 2


Relationships:
none : 6
entry_​version_​of : 1
mapped_​to : 3
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_PHEN10img genetic aspects C0017399
DISO_to_ANAT7img Brain C0006104
DISO_to_CHEM7img Amyloid beta-Peptides C0078939
DISO_to_CHEM6img Amyloid beta-Protein Precursor C0085151
DISO_to_DISO6img Cerebral Hemorrhage C2937358
DISO_to_DISOmapped_toimg CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED C2751536
DISO_to_DISOmapped_toimg CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE C1867773
DISO_to_DISOentry_version_ofimg Cerebral Amyloid Angiopathy, Familial C0268393
DISO_to_DISOmapped_toimg Finnish type amyloidosis C1527170
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268393Cerebral Amyloid Angiopathy, Familial0self