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Details
Link-It Detail - Disease - Diabetes Mellitus, Type 1
Debug Stats
  • ### Total Build Time: 533 ms 33.062 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 348 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 456 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=65 ms Completed: 65 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 990 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 554 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.063 KB
  • CONCEPT_RELATIONSHIPS gt=415 ms Completed: 415 ms rowSize= 16.331 KB
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 9.004 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Diabetes Mellitus, Type 1 C0011854
Definition (1)
A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Diabetes Mellitus C0011849
img Autoimmune Diseases C0004364
Children (1)
img Wolfram Syndrome C0043207
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Diabetes Mellitus C00118493img Diabetes Mellitus C0011849
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255175img Diabetes Mellitus C0011849
img Immune System Diseases C0021053img Autoimmune Diseases C00043643img Autoimmune Diseases C0004364
Relationships (455)

Relation Types:
diso_​to_​anat : 49
diso_​to_​chem : 220
diso_​to_​diso : 142
diso_​to_​gene : 9
diso_​to_​phen : 3
diso_​to_​phys : 32


Relationships:
none : 280
associated_​with : 16
expanded_​form_​of : 1
gene_​associated_​with_​disease : 6
gene_​product_​malfunction_​associated_​with_​disease : 2
inheritance_​type_​of : 1
is_​associated_​anatomic_​site_​of : 2
is_​normal_​cell_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
isa : 11
manifestation_​of : 11
mapped_​to : 2
may_​treat : 114
related_​to : 5
use : 1
Page Size
Current 25
  Page 1 of 19
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT2160img In Blood C0005768
DISO_to_DISO2071img Complication Aspects C1171258
DISO_to_DISO1676img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_ANAT1544img In Blood C0005768
DISO_to_DISO1474img Complication Aspects C1171258
DISO_to_PHEN1393img genetic aspects C0017399
DISO_to_CHEM1319img Insulin C0021641
DISO_to_DISO1271img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_PHEN1241img genetic aspects C0017399
DISO_to_CHEM1032img Insulin C0021641
DISO_to_CHEM851img Agents, Antihyperglycemic C0020616
DISO_to_CHEM732img Blood Glucose C0005802
DISO_to_CHEM538img Agents, Antihyperglycemic C0020616
DISO_to_CHEM484img Blood Glucose C0005802
DISO_to_ANAT392img Insulin-Secreting Cells C0030281
DISO_to_DISO378img Diabetic Nephropathies C0011881
DISO_to_ANAT373img Islets of Langerhans C0022131
DISO_to_DISO362img Hypoglycemia C0020615
DISO_to_DISO331img Diabetic Nephropathies C0011881
DISO_to_CHEM310img Glycosylated hemoglobin A C0019018
DISO_to_CHEM306img Abs - Autoantibodies C0004358
DISO_to_CHEM302img Abs - Autoantibodies C0004358
DISO_to_DISO269img Angiopathies, Diabetic C0011875
DISO_to_DISO269img Hypoglycemia C0020615
DISO_to_DISO261img DIABETES MELLITUS EXPER C0011853
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanAPOA5116519apolipoprotein A-V
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanFOXP350943forkhead box P3
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanHNF1A6927HNF1 homeobox A
img OMIM, Score=844, UMLKSK CUI: C0011854
HumanMEF2A4205myocyte enhancer factor 2A
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanPDX13651pancreatic and duodenal homeobox 1
img OMIM, Score=882, UMLKSK CUI: C0011854
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanHLA-DQA13117
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanCTNS1497cystinosin, lysosomal cystine transporter
img OMIM, Score=1000, UMLKSK CUI: C0011854
HumanAIRE326autoimmune regulator
img OMIM, Score=1000, UMLKSK CUI: C0011854
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011854Diabetes Mellitus, Type 10self