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Details
Link-It Detail - Disease - Diabetes Insipidus
Debug Stats
  • ### Total Build Time: 194 ms 38.045 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 355 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=0 Completed: 0 ms rowSize= 987 bytes
  • CONCEPT_CHILDREN gt=16 ms Completed: 16 ms rowSize= 1.418 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 5.372 KB
  • CONCEPT_RELATIONSHIPS gt=142 ms Completed: 142 ms rowSize= 14.059 KB
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 14.196 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Diabetes Insipidus C0011848
Definition (1)
metabolic disorder due to injury of the neurohypophyseal system; results in deficient quanity of antidiuretic hormone being released or produced, failure of tubular reabsorption of water in the kidney.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Pituitary Diseases C0032002
img Kidney Diseases C0022658
Children (3)
img Diabetes Insipidus, Neurogenic C0687720
img Diabetes Insipidus, Nephrogenic C0162283
img Wolfram Syndrome C0043207
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076826img Pituitary Diseases C0032002
img Endocrine System Diseases C0014130img Pituitary Diseases C00320023img Pituitary Diseases C0032002
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208875img Kidney Diseases C0022658
img Male Urogenital Diseases C1720894img Urologic Diseases C00420754img Kidney Diseases C0022658
Relationships (58)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 17
diso_​to_​diso : 32
diso_​to_​gene : 4
diso_​to_​phen : 2


Relationships:
none : 25
classifies : 1
clinically_​similar : 1
gene_​associated_​with_​disease : 4
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 5
mapped_​to : 8
may_​diagnose : 2
may_​treat : 10
related_​to : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO38img Complication Aspects C1171258
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_DISO17img Pituitary Neoplasms C0032019
DISO_to_DISO16img Pituitary Neoplasms C0032019
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_CHEM14img Deamino Arginine Vasopressin C0011701
DISO_to_DISO14img Pregnancy Complications C0032962
DISO_to_CHEM11img Vasopressins C0042413
DISO_to_ANAT10img Pituitary Gland C0032005
DISO_to_DISO10img COMPL POSTOP C0032787
DISO_to_DISO10img Hypopituitarism C0020635
DISO_to_DISO10img chemically induced C0007994
DISO_to_PHEN10img genetic aspects C0017399
DISO_to_DISO9img Histiocytosis, Langerhans-Cell C0019621
DISO_to_DISO9img Pregnancy Complications C0032962
DISO_to_DISO8img COMPL POSTOP C0032787
DISO_to_DISO8img Pituitary Diseases C0032002
DISO_to_CHEM7img Agents, Renal C0035064
DISO_to_DISO7img Histiocytosis, Langerhans-Cell C0019621
DISO_to_DISO7img chemically induced C0007994
DISO_to_ANAT6img Pituitary Gland C0032005
DISO_to_CHEM6img Deamino Arginine Vasopressin C0011701
DISO_to_CHEM6img Receptors, Vasopressin C0078077
DISO_to_DISO6img Increased urine volume C0032617
DISO_to_DISO6img Lung Neoplasms C0024121
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanARL684100ADP-ribosylation factor-like 6
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS1079738Bardet-Biedl syndrome 10
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS755212Bardet-Biedl syndrome 7
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanMKS154903Meckel syndrome, type 1
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS927241Bardet-Biedl syndrome 9
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanTRIM3222954tripartite motif containing 32
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanTP638626tumor protein p63
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanMKKS8195McKusick-Kaufman syndrome
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0011848
HumanWFS17466Wolfram syndrome 1 (wolframin)
img OMIM, Score=1000, UMLKSK CUI: C0011848
HumanCANX821calnexin
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS4585Bardet-Biedl syndrome 4
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS2583Bardet-Biedl syndrome 2
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanBBS1582Bardet-Biedl syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanAVPR2554arginine vasopressin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanAVP551arginine vasopressin
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanARHGAP4393Rho GTPase activating protein 4
INFERRED, Score=800, UMLKSK CUI: C0011848
HumanAQP2359aquaporin 2 (collecting duct)
INFERRED, Score=800, UMLKSK CUI: C0011848
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011848Diabetes Insipidus0self