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Details
Link-It Detail - Disease - Complete trisomy 18 syndrome
Debug Stats
  • ### Total Build Time: 26 ms 17.716 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 257 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=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=22 ms Completed: 22 ms rowSize= 13.308 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 2.579 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Complete trisomy 18 syndrome C0152096
Definition (1)
A chromosomal abnormality consisting of the presence of a third copy of chromosome 18 in somatic cells.
Relationships (37)

Relation Types:
diso_​to_​diso : 37


Relationships:
classifies : 2
disease_​may_​have_​cytogenetic_​abnormality : 27
isa : 1
mapped_​to : 7
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmapped_toimg 18 P minus syndrome C0265473
DISO_to_DISOmapped_toimg 18 Q minus syndrome C0265474
DISO_to_DISOclassifiesimg All other congenital anomalies C0810365
DISO_to_DISOmapped_toimg Anomaly of chromosome pair 18 C0265470
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg BALT Lymphoma C1367652
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Bladder MALT Lymphoma C1511194
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Borrelia Burgdoferi-Associated Cutaneous Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue C1706987
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Breast MALT lymphoma C1332633
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg C-MALT C1367653
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Campylobacter Jejuni-Associated Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma C1707245
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Chlamydia Psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma C1707385
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Colon MALT Lymphoma C1333096
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Colorectal MALT Lymphoma C3272830
DISO_to_DISOmapped_toimg Complete trisomy 18 syndrome C0152096
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Dural Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue C3272487
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Esophageal MALT Lymphoma C2987269
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Refractory C0856011
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage I C0856012
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage II C0856013
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage III C0856014
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage IV C0856015
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Gastric MALT Lymphoma C1333782
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Helicobacter Pylori-Associated Gastric MALT C1333952
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Hepatic MALToma C1333972
DISO_to_DISOdisease_may_have_cytogenetic_abnormalityimg Lymphoma, B-Cell, Marginal Zone C0242647
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanADAM128038ADAM metallopeptidase domain 12
img GENERIF, Score=1000, Pubmed Id: 17701664, UMLKSK CUI: C0152096
HumanLEP3952leptin
img GENERIF, Score=1000, Pubmed Id: 11920898, UMLKSK CUI: C0152096
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0152096Complete trisomy 18 syndrome0self