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Details
Link-It Detail - Disease - Hypohidrosis
Debug Stats
  • ### Total Build Time: 139 ms 20.554 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 363 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 230 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=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=97 ms Completed: 97 ms rowSize= 9.828 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 6.723 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hypohidrosis C0020620
HYPHIDROSIS
Definition (1)
Reduced sweating. Causes include burns, dehydration, radiation, and leprosy.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Sweat Gland Diseases C0038986
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Sweat Gland Diseases C0038986
Relationships (23)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 19
diso_​to_​phen : 2


Relationships:
none : 13
associated_​with : 1
isa : 5
location_​of : 1
mapped_​to : 3
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO26img Complication Aspects C1171258
DISO_to_DISO19img Ectodermal Dysplasia C0013575
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_DISO12img Autonomic Nervous System Diseases C1145628
DISO_to_DISO12img Ectodermal Dysplasia C0013575
DISO_to_DISO11img chemically induced C0007994
DISO_to_PHEN11img genetic aspects C0017399
DISO_to_DISO10img Flushing C0016382
DISO_to_DISO9img Pain Insensitivity, Congenital C0002768
DISO_to_ANAT8img Skin C1123023
DISO_to_DISO8img Congenital Pain Insensitivity C0002768
DISO_to_DISO8img chemically induced C0007994
DISO_to_ANATlocation_ofimg Sweat Glands C0038989
DISO_to_DISOmapped_toimg Ameloonychohypohidrotic syndrome C1863006
DISO_to_DISOassociated_withimg Anhidrosis C0003028
DISO_to_DISOisaimg Ectodermal syndrome with hair-sweating defects C1274212
DISO_to_DISOisaimg Ectodermal syndrome with hair-tooth-sweating defects C1274211
DISO_to_DISOisaimg Fleck syndrome C0406721
DISO_to_DISOmapped_toimg Franceschetti-Jadassohn syndrome C0343111
DISO_to_DISOmapped_toimg Harlequin syndrome C2029348
DISO_to_DISOisaimg Helwig-Larsen Ludvigsen syndrome C0406746
DISO_to_DISOisaimg Segmental hypohidrosis C0393914
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanEDARADD128178EDAR-associated death domain
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanEDAR10913ectodysplasin A receptor
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanTP638626tumor protein p63
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanPVRL15818poliovirus receptor-related 1 (herpesvirus entry mediator C)
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanKRT143861keratin 14
img OMIM, Score=1000, UMLKSK CUI: C0020620
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanGLA2717galactosidase, alpha
img OMIM, Score=1000, UMLKSK CUI: C0020620
HumanEDA1896ectodysplasin A
img OMIM, Score=1000, UMLKSK CUI: C0020620
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020620Hypohidrosis0self