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Details
Link-It Detail - Human Phenotype - Abnormality of the fibula
Debug Stats
  • ### Total Build Time: 47 ms 30.804 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 3.010 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.084 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=24 ms Completed: 24 ms rowSize= 23.917 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the fibula HP:0002991
Parents (1)
img Abnormality of the calf HP:0002981
Children (9)
img Curvatures of the femur, tibia, fibula HP:0002976
img Synostosis involving the fibula HP:0005928
img Disproportionately long fibulae HP:0003085
img Aplasia/Hypoplasia of the fibula HP:0006492
img Tibiofibular diastasis HP:0100535
img Fibular overgrowth HP:0003099
img Fibular duplication HP:0010503
img Increased fibular diameter HP:0012107
img Fibular bowing HP:0010502
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the calf HP:0002981
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the calf HP:0002981
Genes (35)

Species:
human : 35
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMIPOL1145282mirror-image polydactyly 1
img HP RolledUp, OMIM ID: 135750
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img HP RolledUp, OMIM ID: 241530
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanCANT1124583calcium activated nucleotidase 1
img HP RolledUp, OMIM ID: 251450
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
img HP RolledUp, OMIM ID: 600081
HumanDYNC2H179659dynein, cytoplasmic 2, heavy chain 1
img HP RolledUp, OMIM ID: 615087
HumanLMBR164327limb development membrane protein 1
img HP RolledUp, OMIM ID: 200500
HumanSMOC164093SPARC related modular calcium binding 1
img HP TAS, OMIM ID: 206920
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanSLC35D123169solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
img HP TAS, OMIM ID: 269250
HumanGPC610082glypican 6
img HP RolledUp, OMIM ID: 258315
HumanRBM8A9939RNA binding motif protein 8A
img HP RolledUp, OMIM ID: 274000
HumanPAPSS290603'-phosphoadenosine 5'-phosphosulfate synthase 2
img HP RolledUp, OMIM ID: 603005
HumanGDF58200growth differentiation factor 5
img HP TAS, OMIM ID: 200700
img HP RolledUp, OMIM ID: 201250
img HP RolledUp, OMIM ID: 228900
HumanWNT7A7476wingless-type MMTV integration site family, member 7A
img HP TAS, OMIM ID: 228930
img HP TAS, OMIM ID: 276820
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanTBX156913T-box 15
img HP RolledUp, OMIM ID: 260660
HumanSOX96662SRY (sex determining region Y)-box 9
img HP RolledUp, OMIM ID: 114290
HumanSHOX6473short stature homeobox
img HP TAS, OMIM ID: 249700
img HP RolledUp, OMIM ID: 127300
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
img HP RolledUp, OMIM ID: 307800
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img HP RolledUp, OMIM ID: 300009
HumanDDR24921discoidin domain receptor tyrosine kinase 2
img HP RolledUp, OMIM ID: 271665
HumanIHH3549indian hedgehog
img HP RolledUp, OMIM ID: 607778
HumanFLNB2317filamin B, beta
img HP RolledUp, OMIM ID: 108720
img HP RolledUp, OMIM ID: 112310
HumanFLNA2316filamin A, alpha
img HP TAS, OMIM ID: 304120
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002991Abnormality of the fibula0self