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Details
Link-It Detail - Disease - Diabetes Insipidus, Neurogenic
Debug Stats
  • ### Total Build Time: 89 ms 23.854 KB
  • CONCEPT_NAME gt=26 ms Completed: 26 ms rowSize= 414 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Diabetes Insipidus, Neurogenic C0687720
Central Diabetes Insipidus
Definition (1)
A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Diabetes Insipidus C0011848
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076827img Diabetes Insipidus C0011848
img Endocrine System Diseases C0014130img Pituitary Diseases C00320024img Diabetes Insipidus C0011848
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208876img Diabetes Insipidus C0011848
img Male Urogenital Diseases C1720894img Urologic Diseases C00420755img Diabetes Insipidus C0011848
Relationships (18)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 6
diso_​to_​diso : 8
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 12
clinically_​similar : 1
expanded_​form_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 2
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN34img genetic aspects C0017399
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_DISO21img Complication Aspects C1171258
DISO_to_PHEN19img genetic aspects C0017399
DISO_to_CHEM17img Vasopressins C0042413
DISO_to_CHEM15img Arginine Vasopressin C0003779
DISO_to_CHEM14img Neurohypophysin C0027900
DISO_to_PHYS13img Mutation C0026882
DISO_to_CHEM12img Precursors, Protein C0033665
DISO_to_CHEM12img Protein Precursors C0033665
DISO_to_CHEM11img Deamino Arginine Vasopressin C0011701
DISO_to_DISO11img Hypopituitarism C0020635
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Endocrine System C0014136
DISO_to_DISOexpanded_form_ofimg Central Diabetes Insipidus C0687720
DISO_to_DISOclinically_similarimg Diabetes Insipidus C0011848
DISO_to_DISOmapped_toimg Diabetes insipidus cranial type C2931069
DISO_to_DISOisaimg Familial central diabetes insipidus C0342394
DISO_to_DISOisaimg Secondary diabetes insipidus C0271593
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanTP638626tumor protein p63
img OMIM, Score=1000, UMLKSK CUI: C0687720
HumanAVP551arginine vasopressin
img OMIM, Score=882, UMLKSK CUI: C0687720
img OMIM, Score=1000, UMLKSK CUI: C0687720
img GENERIF, Score=884, Pubmed Id: 12359138, UMLKSK CUI: C0687720
img GAD, Score=1000, Pubmed Id: 8045958, UMLKSK CUI: C0687720
img GENERIF, Score=884, Pubmed Id: 12107248, UMLKSK CUI: C0687720
img GENERIF, Score=717, Pubmed Id: 18807739, UMLKSK CUI: C0687720
img GENERIF, Score=884, Pubmed Id: 11980620, UMLKSK CUI: C0687720
img GAD, Score=1000, Pubmed Id: 12359138, UMLKSK CUI: C0687720
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0687720Diabetes Insipidus, Neurogenic0self