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Details
Link-It Detail - Human Phenotype - Abnormality of the gallbladder
Debug Stats
  • ### Total Build Time: 26 ms 28.159 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 205 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 201 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 454 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.351 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.169 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 22.631 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the gallbladder HP:0005264
Definition (1)
An abnormality of the `gallbladder` (FMA:7202).
Parents (1)
img Abnormality of the biliary system HP:0004297
Children (7)
img Hypoplasia of the gallbladder HP:0005233
img Gallbladder dysfunction HP:0005609
img Bilobate gallbladder HP:0005608
img Cholelithiasis HP:0001081
img Cholecystitis HP:0001082
img Aplasia/Hypoplasia of the gallbladder HP:0011466
img Neoplasm of the gallbladder HP:0100575
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the biliary system HP:0004297
Genes (39)

Species:
human : 39
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanRFX6222546regulatory factor X, 6
img HP RolledUp, OMIM ID: 601346
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
img HP RolledUp, OMIM ID: 611465
HumanDHS10774dehydrated hereditary stomatocytosis
img HP RolledUp, OMIM ID: 194380
HumanSEC23B10483Sec23 homolog B (S. cerevisiae)
img HP RolledUp, OMIM ID: 224100
HumanPIEZO19780piezo-type mechanosensitive ion channel component 1
img HP RolledUp, OMIM ID: 194380
HumanABCB118647ATP-binding cassette, sub-family B (MDR/TAP), member 11
img HP RolledUp, OMIM ID: 605479
HumanOGS28221Opitz G syndrome, type II
img HP TAS, OMIM ID: 145410
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img HP TAS, OMIM ID: 194190
HumanWHCR7467Wolf-Hirschhorn syndrome chromosome region
img HP TAS, OMIM ID: 194190
HumanUROS7390uroporphyrinogen III synthase
img HP RolledUp, OMIM ID: 263700
HumanTPI17167triosephosphate isomerase 1
img HP RolledUp, OMIM ID: 190450
HumanTHAS7055thoracoabdominal syndrome
img HP TAS, OMIM ID: 313850
HumanTBX16899T-box 1
img HP RolledUp, OMIM ID: 188400
HumanSTK116794serine/threonine kinase 11
img HP TAS, OMIM ID: 175200
HumanSC5D6309sterol-C5-desaturase
img HP RolledUp, OMIM ID: 607330
HumanPEX195824peroxisomal biogenesis factor 19
img HP RolledUp, OMIM ID: 614886
HumanPKLR5313pyruvate kinase, liver and RBC
img HP RolledUp, OMIM ID: 266200
HumanABCB45244ATP-binding cassette, sub-family B (MDR/TAP), member 4
img HP RolledUp, OMIM ID: 600803
HumanPFKM5213phosphofructokinase, muscle
img HP RolledUp, OMIM ID: 232800
HumanHOXD133239homeobox D13
img HP TAS, OMIM ID: 192350
HumanHK13098hexokinase 1
img HP RolledUp, OMIM ID: 235700
HumanHBB3043hemoglobin, beta
img HP RolledUp, OMIM ID: 603903
img HP RolledUp, OMIM ID: 141900
HumanGPI2821glucose-6-phosphate isomerase
img HP RolledUp, OMIM ID: 613470
img HP RolledUp, OMIM ID: 172400
HumanG6PD2539glucose-6-phosphate dehydrogenase
img HP RolledUp, OMIM ID: 305900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005264Abnormality of the gallbladder0self