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Details
Link-It Detail - Disease - Hypogonadism
Debug Stats
  • ### Total Build Time: 535 ms 42.863 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 546 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=9 ms Completed: 9 ms rowSize= 553 bytes
  • CONCEPT_CHILDREN gt=19 ms Completed: 19 ms rowSize= 1.813 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.507 KB
  • CONCEPT_RELATIONSHIPS gt=458 ms Completed: 458 ms rowSize= 14.536 KB
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 22.262 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypogonadism C0020619
Definition (1)
Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Gonadal Disorders C0018050
Children (4)
img Klinefelter Syndrome C0022735
img Sexual Infantilism C0242341
img Eunuchism C0238117
img Kallmann Syndrome C0162809
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Gonadal Disorders C00180503img Gonadal Disorders C0018050
Relationships (272)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 197
diso_​to_​diso : 58
diso_​to_​phen : 2
diso_​to_​phys : 7


Relationships:
none : 50
disease_​has_​associated_​disease : 1
is_​associated_​anatomic_​site_​of : 2
is_​primary_​anatomic_​site_​of_​disease : 2
isa : 8
mapped_​to : 28
may_​treat : 180
use : 1
Page Size
Current 25
  Page 1 of 11
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM342img Testosterone C0039601
DISO_to_CHEM213img Testosterone C0039601
DISO_to_ANAT203img In Blood C0005768
DISO_to_DISO195img Complication Aspects C1171258
DISO_to_PHEN155img genetic aspects C0017399
DISO_to_DISO130img Complication Aspects C1171258
DISO_to_ANAT116img In Blood C0005768
DISO_to_CHEM109img Androgens C0002844
DISO_to_PHEN106img genetic aspects C0017399
DISO_to_CHEM77img Androgens C0002844
DISO_to_DISO62img Erectile Dysfunction C0242350
DISO_to_PHYS46img Aging C0001811
DISO_to_DISO40img Metabolic Syndrome X C0524620
DISO_to_DISO37img chemically induced C0007994
DISO_to_DISO35img Erectile Dysfunction C0242350
DISO_to_PHYS34img Aging C0001811
DISO_to_DISO32img Prostatic Neoplasms C0033578
DISO_to_CHEM31img Gonadorelin C0023610
DISO_to_PHYS31img Mutation C0026882
DISO_to_CHEM30img Gonadotropins C0018061
DISO_to_DISO29img Infertility, Male C0021364
DISO_to_DISO27img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_CHEM25img Gonadotropin-Releasing Hormone Receptor C0034811
DISO_to_CHEM25img Receptors, LHRH C0034811
DISO_to_DISO25img Obesity C0028754
Genes (64)

Species:
human : 64
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPALM2-AKAP2445815
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanBBS12166379Bardet-Biedl syndrome 12
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanBBS5129880Bardet-Biedl syndrome 5
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanPROKR2128674prokineticin receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanTTC8123016tetratricopeptide repeat domain 8
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanTMEM6791147transmembrane protein 67
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanKISS1R84634KISS1 receptor
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanARL684100ADP-ribosylation factor-like 6
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanDCAF1780067DDB1 and CUL4 associated factor 17
img GENERIF, Score=861, Pubmed Id: 19026396, UMLKSK CUI: C0020619
HumanBBS1079738Bardet-Biedl syndrome 10
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanPROK260675prokineticin 2
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanBBS755212Bardet-Biedl syndrome 7
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanBBS927241Bardet-Biedl syndrome 9
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanUQCRQ27089ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanRAB3GAP225782RAB3 GTPase activating protein subunit 2 (non-catalytic)
INFERRED, Score=800, UMLKSK CUI: C0020619
HumanTRIM3222954tripartite motif containing 32
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanRECQL49401RecQ protein-like 4
img OMIM, Score=1000, UMLKSK CUI: C0020619
HumanNMT29397N-myristoyltransferase 2
img GENERIF, Score=1000, Pubmed Id: 17568424, UMLKSK CUI: C0020619
HumanCTDP19150CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
INFERRED, Score=800, UMLKSK CUI: C0020619
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020619Hypogonadism0self