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Details
Link-It Detail - Disease - PEELING SKIN SYNDROME
Debug Stats
  • ### Total Build Time: 40 ms 10.747 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=32 ms Completed: 32 ms rowSize= 7.317 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 1.872 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
PEELING SKIN SYNDROME C1849193
Relationships (17)

Relation Types:
diso_​to_​diso : 17


Relationships:
alias_​of : 1
manifestation_​of : 16
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Acral form of skin peeling limited to hands and feet (609796) C2678354
DISO_to_DISOmanifestation_ofimg Asthma C0004096
DISO_to_DISOmanifestation_ofimg Caused by mutation in the corneodesmosin gene (CDSN, 602593.0003) C3279429
DISO_to_DISOmanifestation_ofimg Cleavage at junction of stratum corneum and stratum granulosum C2678352
DISO_to_DISOmanifestation_ofimg Elevated levels of serum IgE C3279428
DISO_to_DISOmanifestation_ofimg Fragile hair C1970705
DISO_to_DISOmanifestation_ofimg Generalized erythema (inflammatory type B) C2678349
DISO_to_DISOmanifestation_ofimg Low plasma tryptophan (inflammatory type B) C2678347
DISO_to_DISOmanifestation_ofimg Oncholysis, distal C2678353
DISO_to_DISOmanifestation_ofimg Onset at birth C1836142
DISO_to_DISOalias_ofimg PEELING SKIN SYNDROME C1849193
DISO_to_DISOmanifestation_ofimg Pruritus (inflammatory type B) C2678350
DISO_to_DISOmanifestation_ofimg See also peeling skin syndrome, acral type (609796) C2678356
DISO_to_DISOmanifestation_ofimg Short stature C0349588
DISO_to_DISOmanifestation_ofimg Superficial generalized lifelong skin peeling (sparing palms and soles) C2678348
DISO_to_DISOmanifestation_ofimg Two subtypes noninflammatory type A and inflammatory type B C2678355
DISO_to_DISOmanifestation_ofimg Vesicular lesions (inflammatory type B) C2678351
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanTGM59333transglutaminase 5
img OMIM, Score=909, UMLKSK CUI: C1849193
img OMIM, Score=814, UMLKSK CUI: C1849193
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1849193PEELING SKIN SYNDROME0self