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Details
Link-It Detail - Disease - Hyperostosis Frontalis Interna
Debug Stats
  • ### Total Build Time: 46 ms 12.086 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 325 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 988 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.770 KB
  • CONCEPT_RELATIONSHIPS gt=21 ms Completed: 21 ms rowSize= 4.967 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 1.335 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperostosis Frontalis Interna C0020494
Definition (1)
A condition of unknown etiology characterized by thickening of the inner table of the frontal bone of the skull. It is seen more often in females and is usually bilateral.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Hyperostosis C0020492
img Osteochondrodysplasias C0029422
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Bone Diseases C00059404img Hyperostosis C0020492
img Musculoskeletal Diseases C0026857img Bone Diseases C00059405img Osteochondrodysplasias C0029422
Relationships (9)

Relation Types:
diso_​to_​anat : 5
diso_​to_​diso : 3
diso_​to_​phen : 1


Relationships:
none : 5
is_​associated_​anatomic_​site_​of : 2
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT4img Bone structure of cranium C0037303
DISO_to_ANAT4img Bone structure of face C0015455
DISO_to_ANAT3img Frontal Bone C0016732
DISO_to_DISO3img HYPERPARATHYROIDISM SECOND C0020503
DISO_to_PHEN3img genetic aspects C0017399
DISO_to_ANATis_associated_anatomic_site_ofimg Connective and Soft Tissue C1516798
DISO_to_ANATis_associated_anatomic_site_ofimg Skeletal bone C0262950
DISO_to_DISOpermuted_term_ofimg HYPEROSTOSIS FRONTALIS INTERNA C0020494
DISO_to_DISOmapped_toimg Hyperostosis frontalis interna, obesity, shortness and cognitive impairment C2931890
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0020494
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020494Hyperostosis Frontalis Interna0self