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Details
Link-It Detail - Human Phenotype - Abnormality of the peritoneum
Debug Stats
  • ### Total Build Time: 31 ms 21.842 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 204 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 200 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=4 ms Completed: 4 ms rowSize= 787 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.687 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 3.031 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 14.793 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the peritoneum HP:0002585
Definition (1)
An abnormality of the `peritoneum` (FMA:9584).
Parents (2)
img Abnormality of the intestine HP:0002242
img Abnormality of the abdominal organs HP:0002012
Children (5)
img Retroperitoneal fibrosis HP:0005200
img Peritoneal mesothelioma HP:0100003
img Peritonitis HP:0002586
img Hemoperitoneum HP:0011854
img Peritoneal abscess HP:0100592
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the intestine HP:0002242
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the intestine HP:0002242
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the abdominal organs HP:0002012
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP TAS, OMIM ID: 613024
HumanMMS338340Malignant mesothelioma, susceptibility to
img HP TAS, OMIM ID: 156240
HumanSLC29A355315solute carrier family 29 (equilibrative nucleoside transporter), member 3
img HP RolledUp, OMIM ID: 602782
HumanSOX1854345SRY (sex determining region Y)-box 18
img HP TAS, OMIM ID: 607823
HumanBCL108915B-cell CLL/lymphoma 10
img HP TAS, OMIM ID: 156240
img HP TAS, OMIM ID: 613024
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
img HP TAS, OMIM ID: 223900
HumanWT17490Wilms tumor 1
img HP TAS, OMIM ID: 156240
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
img HP RolledUp, OMIM ID: 142680
HumanTHM7063thymoma
img HP TAS, OMIM ID: 274230
HumanMVK4598mevalonate kinase
img HP RolledUp, OMIM ID: 260920
HumanMEFV4210Mediterranean fever
img HP RolledUp, OMIM ID: 249100
img HP RolledUp, OMIM ID: 134610
HumanJAK23717Janus kinase 2
img HP RolledUp, OMIM ID: 600880
HumanF52153coagulation factor V (proaccelerin, labile factor)
img HP RolledUp, OMIM ID: 600880
HumanCOL5A21290collagen, type V, alpha 2
img HP RolledUp, OMIM ID: 130000
HumanCOL5A11289collagen, type V, alpha 1
img HP RolledUp, OMIM ID: 130010
img HP RolledUp, OMIM ID: 130000
HumanCOL1A11277collagen, type I, alpha 1
img HP RolledUp, OMIM ID: 130000
HumanAPC324adenomatous polyposis coli
img HP TAS, OMIM ID: 135290
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002585Abnormality of the peritoneum0self