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Details
Link-It Detail - Disease - DIABETES MELLITUS, PERMANENT NEONATAL
Debug Stats
  • ### Total Build Time: 124 ms 18.037 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 372 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=107 ms Completed: 107 ms rowSize= 12.430 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 4.003 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
DIABETES MELLITUS, PERMANENT NEONATAL C1833104
Relationships (35)

Relation Types:
diso_​to_​diso : 35


Relationships:
expanded_​form_​of : 1
manifestation_​of : 32
related_​to : 2
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Absence of pancreatic autoantibodies C1969878
DISO_to_DISOmanifestation_ofimg Anteverted nostrils C1837721
DISO_to_DISOmanifestation_ofimg Axial hypotonia C1853743
DISO_to_DISOmanifestation_ofimg Beta-cell dysfunction C1969875
DISO_to_DISOmanifestation_ofimg Blepharoptosis C0005745
DISO_to_DISOmanifestation_ofimg CLINODACTYLY C0265610
DISO_to_DISOmanifestation_ofimg Caused by mutation in the ATP-binding cassette, subfamily C, member 8 gene (ABCC8, 600509.0016) C1969882
DISO_to_DISOmanifestation_ofimg Caused by mutation in the glucokinase gene (GCK, 138079.0011) C3148989
DISO_to_DISOmanifestation_ofimg Caused by mutation in the potassium channel, inwardly rectifying, subfamily J, member 11 gene (KCNJ11, 600937.0002) C3148990
DISO_to_DISOrelated_toimg DEND C1853564
DISO_to_DISOexpanded_form_ofimg DIABETES MELLITUS, PERMANENT NEONATAL C1833104
DISO_to_DISOrelated_toimg DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES C1833102
DISO_to_DISOmanifestation_ofimg Developmental delay (disorder) C0424605
DISO_to_DISOmanifestation_ofimg Diabetes Mellitus C0011849
DISO_to_DISOmanifestation_ofimg Diabetic peripheral neuropathy in long-standing cases C1969873
DISO_to_DISOmanifestation_ofimg Diagnosis within the first 3 months of life C1969883
DISO_to_DISOmanifestation_ofimg Diffuse hypotonia C1969871
DISO_to_DISOmanifestation_ofimg Downturned mouth C1854116
DISO_to_DISOmanifestation_ofimg EEG shows epileptiform activity C1969872
DISO_to_DISOmanifestation_ofimg Fetal Growth Retardation C0015934
DISO_to_DISOmanifestation_ofimg Hyperglycemia C0020456
DISO_to_DISOmanifestation_ofimg Hypsarrhythmia C0684276
DISO_to_DISOmanifestation_ofimg Ketoacidosis C0220982
DISO_to_DISOmanifestation_ofimg Limb contractures C1969879
DISO_to_DISOmanifestation_ofimg Long philtrum C1865014
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanKCNJ113767potassium inwardly-rectifying channel, subfamily J, member 11
img GENERIF, Score=1000, Pubmed Id: 17923772, UMLKSK CUI: C1833104
img GENERIF, Score=1000, Pubmed Id: 15580558, UMLKSK CUI: C1833104
img GENERIF, Score=1000, Pubmed Id: 18662362, UMLKSK CUI: C1833104
HumanINS3630insulin
img GENERIF, Score=1000, Pubmed Id: 18662362, UMLKSK CUI: C1833104
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1833104DIABETES MELLITUS, PERMANENT NEONATAL0self