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Details
Link-It Detail - Disease - Diabetes Mellitus, Lipoatrophic
Debug Stats
  • ### Total Build Time: 86 ms 15.390 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 356 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= 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= 561 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 11 ms rowSize= 2.805 KB
  • CONCEPT_RELATIONSHIPS gt=43 ms Completed: 43 ms rowSize= 9.910 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Diabetes Mellitus, Lipoatrophic C0011859
Definition (1)
A type of diabetes mellitus that is characterized by severe INSULIN RESISTANCE and LIPODYSTROPHY. The latter may be generalized, partial, acquired, or congenital (LIPODYSTROPHY, CONGENITAL GENERALIZED).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Diabetes Mellitus, Type 2 C0011860
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Diabetes Mellitus C00118494img Diabetes Mellitus, Type 2 C0011860
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255176img Diabetes Mellitus, Type 2 C0011860
Relationships (19)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 6
diso_​to_​diso : 5
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 10
associated_​with : 1
is_​associated_​anatomic_​site_​of : 2
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 1
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN21img genetic aspects C0017399
DISO_to_ANAT7img In Blood C0005768
DISO_to_PHYS5img Mutation C0026882
DISO_to_CHEM4img G Protein gamma Subunit C0887849
DISO_to_CHEM4img GTP-Binding Protein gamma Subunits C0887849
DISO_to_CHEM4img Insulin C0021641
DISO_to_CHEM4img Lamin Type A C0125258
DISO_to_CHEM4img Leptin C0299583
DISO_to_CHEM4img PPAR gamma C0166417
DISO_to_DISO4img Complication Aspects C1171258
DISO_to_ANATis_associated_anatomic_site_ofimg Digestive System C0012240
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Endocrine System C0014136
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Islet Cell C1522529
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Islets of Langerhans C0022131
DISO_to_ANATis_associated_anatomic_site_ofimg Pancreas C0030274
DISO_to_DISOmapped_toimg ACRORENAL FIELD DEFECT, ECTODERMAL DYSPLASIA, AND LIPOATROPHIC DIABETES C0342280
DISO_to_DISOisaimg Congenital total lipoatrophy C1274779
DISO_to_DISOassociated_withimg Diabetes Mellitus C0011849
DISO_to_DISOpermuted_term_ofimg Diabetes Mellitus, Lipoatrophic C0011859
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011859Diabetes Mellitus, Lipoatrophic0self