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Details
Link-It Detail - Disease - Anetoderma
Debug Stats
  • ### Total Build Time: 27 ms 15.390 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 384 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=6 ms Completed: 6 ms rowSize= 998 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.132 KB
  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 4.953 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.230 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anetoderma C1288283
Atrophoderma maculatum
Definition (1)
Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. It can be either primary (idiopathic) or secondary to other skin conditions, PENICILLAMINE use, or premature birth.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Skin Abnormalities C0037268
img Connective Tissue Diseases C0009782
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Skin Abnormalities C0037268
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Skin Abnormalities C0037268
img Skin and Connective Tissue Diseases C0175166img Connective Tissue Diseases C00097823img Connective Tissue Diseases C0009782
Relationships (10)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 8


Relationships:
none : 2
isa : 6
location_​of : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT3img Skin C1123023
DISO_to_DISO3img Complication Aspects C1171258
DISO_to_ANATlocation_ofimg Skin C1123023
DISO_to_DISOpermuted_term_ofimg Anetoderma C1288283
DISO_to_DISOisaimg Anetoderma following chickenpox C1274328
DISO_to_DISOisaimg Anetoderma secondary to lupus erythematosus C1274849
DISO_to_DISOisaimg Anetoderma secondary to syphilis C1274368
DISO_to_DISOisaimg Anetoderma, Primary C0406550
DISO_to_DISOisaimg Anetoderma, Secondary C0406553
DISO_to_DISOisaimg Drug-induced anetoderma C1274993
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
img GENERIF, Score=901, Pubmed Id: 15322982, UMLKSK CUI: C1288283
HumanELOVL46785ELOVL fatty acid elongase 4
img OMIM, Score=882, UMLKSK CUI: C1288283
HumanGBA2629glucosidase, beta, acid
img OMIM, Score=1000, UMLKSK CUI: C1288283
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1288283Anetoderma0self