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Details
Link-It Detail - Human Phenotype - Abnormal feet morphology
Debug Stats
  • ### Total Build Time: 24 ms 17.190 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 443 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.084 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 12.719 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal feet morphology HP:0010611
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the foot HP:0001760
Children (1)
img Minor feet anomalies HP:0010613
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the foot HP:0001760
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the foot HP:0001760
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 605039
HumanABCC910060ATP-binding cassette, sub-family C (CFTR/MRP), member 9
img HP RolledUp, OMIM ID: 239850
HumanZEB29839zinc finger E-box binding homeobox 2
img HP RolledUp, OMIM ID: 235730
HumanPTCH15727patched 1
img HP RolledUp, OMIM ID: 109400
HumanMAP2K25605mitogen-activated protein kinase kinase 2
img HP RolledUp, OMIM ID: 115150
HumanMAP2K15604mitogen-activated protein kinase kinase 1
img HP RolledUp, OMIM ID: 115150
HumanKRAS3845Kirsten rat sarcoma viral oncogene homolog
img HP RolledUp, OMIM ID: 218040
img HP RolledUp, OMIM ID: 115150
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
img HP RolledUp, OMIM ID: 218040
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img HP RolledUp, OMIM ID: 214150
HumanERCC52073excision repair cross-complementing rodent repair deficiency, complementation group 5
img HP RolledUp, OMIM ID: 214150
HumanEP3002033E1A binding protein p300
HumanCREBBP1387CREB binding protein
HumanBRAF673v-raf murine sarcoma viral oncogene homolog B
img HP RolledUp, OMIM ID: 115150
HumanATP2A2488ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
img HP RolledUp, OMIM ID: 124200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010611Abnormal feet morphology0self