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Details
Link-It Detail - Disease - Hypopigmentation Adverse Event
Debug Stats
  • ### Total Build Time: 47 ms 10.485 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 358 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=1 ms Completed: 1 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=10 ms Completed: 10 ms rowSize= 1.467 KB
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 7.435 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypopigmentation Adverse Event C1963139
Relationships (2)

Relation Types:
diso_​to_​diso : 2


Relationships:
isa : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg CTCAE Grade 1 Hypopigmentation C1559120
DISO_to_DISOisaimg CTCAE Grade 2 Hypopigmentation C1559121
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanMLPH79083melanophilin
img GENERIF, Score=694, Pubmed Id: 12897212, UMLKSK CUI: C1963139
HumanUROS7390uroporphyrinogen III synthase
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanUBE3A7337ubiquitin protein ligase E3A
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanCOL4A11282collagen, type IV, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C1963139
HumanATP7A538ATPase, Cu++ transporting, alpha polypeptide
img OMIM, Score=1000, UMLKSK CUI: C1963139
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1963139Hypopigmentation Adverse Event0self