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Details
Link-It Detail - Disease - Diabetes mellitus syndrome in newborn infant
Debug Stats
  • ### Total Build Time: 70 ms 17.062 KB
  • CONCEPT_NAME gt=5 ms Completed: 4 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 568 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= 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=35 ms Completed: 35 ms rowSize= 5.983 KB
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 8.899 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Diabetes mellitus syndrome in newborn infant C0158981
Definition (1)
Transient or permanent diabetes mellitus that affects neonates. It is caused by the inability of the pancreas to secrete sufficient insulin in response to elevated levels of glucose in the blood. The transient diabetes mellitus lasts for weeks or months and may return in adolescence or in adulthood. The permanent diabetes mellitus does not disappear and is caused by mutations in the KCNJ11, GCK, and IPF1 genes.
Relationships (10)

Relation Types:
diso_​to_​anat : 5
diso_​to_​diso : 5


Relationships:
classifies : 2
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 : 2
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
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_DISOisaimg Diabetes mellitus in neonate small for gestational age C0349474
DISO_to_DISOmapped_toimg Diabetes mellitus syndrome in newborn infant C0158981
DISO_to_DISOclassifiesimg Endocrine and metabolic disturbances of fetus and newborn C0810367
DISO_to_DISOclassifiesimg Other perinatal conditions C0554614
DISO_to_DISOisaimg Transitory neonatal diabetes mellitus C0342273
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanZFP57346171ZFP57 zinc finger protein
img OMIM, Score=909, UMLKSK CUI: C0158981
HumanHYMAI57061hydatidiform mole associated and imprinted (non-protein coding)
img OMIM, Score=909, UMLKSK CUI: C0158981
HumanTCF7L26934transcription factor 7-like 2 (T-cell specific, HMG-box)
img GENERIF, Score=1000, Pubmed Id: 17093940, UMLKSK CUI: C0158981
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
img GENERIF, Score=1000, Pubmed Id: 17213273, UMLKSK CUI: C0158981
img GENERIF, Score=923, Pubmed Id: 17446535, UMLKSK CUI: C0158981
HumanPLAGL15325pleiomorphic adenoma gene-like 1
img OMIM, Score=909, UMLKSK CUI: C0158981
HumanKCNJ113767potassium inwardly-rectifying channel, subfamily J, member 11
img GENERIF, Score=1000, Pubmed Id: 17635943, UMLKSK CUI: C0158981
img GENERIF, Score=923, Pubmed Id: 17446535, UMLKSK CUI: C0158981
HumanGCK2645glucokinase (hexokinase 4)
img GENERIF, Score=756, Pubmed Id: 18571549, UMLKSK CUI: C0158981
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0158981Diabetes mellitus syndrome in newborn infant0self