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Details
Link-It Detail - Disease - Hypopituitarism
Debug Stats
  • ### Total Build Time: 244 ms 38.123 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 466 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=15 ms Completed: 15 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 557 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.794 KB
  • CONCEPT_RELATIONSHIPS gt=174 ms Completed: 174 ms rowSize= 13.822 KB
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 18.286 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypopituitarism C0020635
Definition (1)
A condition of diminution or cessation of secretion of one or more hormones from the anterior pituitary gland. This may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Pituitary Diseases C0032002
Children (1)
img Dwarfism, Pituitary C0013338
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
Relationships (78)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 16
diso_​to_​diso : 51
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 43
associated_​with : 2
entry_​version_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 21
location_​of : 1
mapped_​to : 8
use : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO138img Complication Aspects C1171258
DISO_to_DISO135img Complication Aspects C1171258
DISO_to_CHEM123img Human Growth Hormone C0169964
DISO_to_CHEM113img Human Growth Hormone C0169964
DISO_to_ANAT91img In Blood C0005768
DISO_to_ANAT79img In Blood C0005768
DISO_to_PHEN77img genetic aspects C0017399
DISO_to_DISO59img Brain Injuries C0270611
DISO_to_ANAT56img Pituitary Gland C0032005
DISO_to_CHEM50img Growth Hormone C0037663
DISO_to_DISO48img Brain Injuries C0270611
DISO_to_DISO46img Pituitary Neoplasms C0032019
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_CHEM36img Pituitary Hormones C0032015
DISO_to_ANAT29img Pituitary Gland C0032005
DISO_to_CHEM29img Homeo Domain Proteins C0242617
DISO_to_CHEM29img Homeodomain Proteins C0242617
DISO_to_DISO25img Pituitary Neoplasms C0032019
DISO_to_CHEM22img Growth Hormone C0037663
DISO_to_CHEM18img TRANSCRIPTION FACTOR C0040648
DISO_to_DISO18img Adenoma C0001430
DISO_to_DISO18img Adrenal Insufficiency C0001623
DISO_to_ANAT15img Pituitary Gland, Anterior C0032008
DISO_to_CHEM15img Homeo Domain Proteins C0242617
DISO_to_PHYS15img Mutation C0026882
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanLIPI149998lipase, member I
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanAPOA5116519apolipoprotein A-V
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanCSMD3114788CUB and Sushi multiple domains 3
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanLHX489884LIM homeobox 4
img GENERIF, Score=861, Pubmed Id: 18445675, UMLKSK CUI: C0020635
HumanPREPL9581prolyl endopeptidase-like
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanHESX18820HESX homeobox 1
img GENERIF, Score=1000, Pubmed Id: 17148560, UMLKSK CUI: C0020635
HumanSOX36658SRY (sex determining region Y)-box 3
img GENERIF, Score=1000, Pubmed Id: 15800844, UMLKSK CUI: C0020635
HumanSIX36496SIX homeobox 3
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanSHH6469sonic hedgehog
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanSRSF26427serine/arginine-rich splicing factor 2
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanSRSF16426serine/arginine-rich splicing factor 1
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanRP16101retinitis pigmentosa 1 (autosomal dominant)
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanPROP15626PROP paired-like homeobox 1
img GENERIF, Score=1000, Pubmed Id: 12717343, UMLKSK CUI: C0020635
HumanPOU1F15449POU class 1 homeobox 1
img GENERIF, Score=901, Pubmed Id: 15928241, UMLKSK CUI: C0020635
img GENERIF, Score=1000, Pubmed Id: 12717343, UMLKSK CUI: C0020635
HumanLEP3952leptin
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanGLI32737GLI family zinc finger 3
img OMIM, Score=1000, UMLKSK CUI: C0020635
HumanGLI22736GLI family zinc finger 2
img GENERIF, Score=861, Pubmed Id: 14581620, UMLKSK CUI: C0020635
HumanGHR2690growth hormone receptor
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanGH12688growth hormone 1
INFERRED, Score=800, UMLKSK CUI: C0020635
HumanBMP4652bone morphogenetic protein 4
img OMIM, Score=1000, UMLKSK CUI: C0020635
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020635Hypopituitarism0self