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Details
Link-It Detail - Human Phenotype - Abnormality of the abdominal wall
Debug Stats
  • ### Total Build Time: 40 ms 34.017 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 230 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=5 ms Completed: 5 ms rowSize= 780 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 4.930 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.026 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 23.699 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the abdominal wall HP:0004298
Definition (1)
The presence of any abnormality affecting the `abdominal wall` (FMA:259054).
Parents (2)
img Abnormality of the abdomen HP:0001438
img Abnormality of the musculature HP:0003011
Children (15)
img Partial abdominal muscle agenesis HP:0005243
img Abnormality of the umbilicus HP:0001551
img Cloacal exstrophy HP:0010475
img Hernia of the abdominal wall HP:0004299
img Lax abdominal musculature HP:0004873
img Omphalocele HP:0001539
img Diastasis recti HP:0001540
img Aplasia/Hypoplasia of the abdominal wall musculature HP:0010318
img Abdominal wall muscle weakness HP:0009023
img Exstrophy HP:0100548
img Gastroschisis HP:0001543
img Prune belly HP:0004392
img Protuberant abdomen due to muscle weakness HP:0001546
img Abdominal wall defect HP:0010866
img Abnormality of the abdominal musculature HP:0010991
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the abdomen HP:0001438
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the musculature HP:0003011
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the musculature HP:0003011
Genes (268)

Species:
human : 268
Page Size
Current 25
  Page 1 of 11
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOPHLC101290499Omphalocele due to duplication of 1p31.3
img HP RolledUp, OMIM ID: 310980
img HP RolledUp, OMIM ID: 164750
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanDUPXQ28100415893Chromosome Xq28 duplication syndrome
img HP RolledUp, OMIM ID: 300815
HumanDUP17P13.3100379203
img HP RolledUp, OMIM ID: 613215
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanIH100188864Hemihypertrophy
img HP RolledUp, OMIM ID: 235000
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanKIF7374654kinesin family member 7
img HP RolledUp, OMIM ID: 200990
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanMMS338340Malignant mesothelioma, susceptibility to
img HP TAS, OMIM ID: 156240
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004298Abnormality of the abdominal wall0self