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Details
Link-It Detail - Human Phenotype - Abnormality of the foot musculature
Debug Stats
  • ### Total Build Time: 22 ms 32.331 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 210 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 796 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.710 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 4.937 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 23.528 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the foot musculature HP:0001436
Parents (2)
img Abnormality of the musculature of the lower limbs HP:0001437
img Abnormality of the foot HP:0001760
Children (5)
img Flexion limitation of toes HP:0008116
img Amyotrophy of ankle musculature HP:0009031
img Foot dorsiflexor weakness HP:0009027
img Toe extensor amyotrophy HP:0011916
img Foot drop HP:0003377
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the musculature of the lower limbs HP:0001437
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the musculature of the lower limbs HP:0001437
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the musculature of the lower limbs HP:0001437
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the foot HP:0001760
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the foot HP:0001760
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
img HP RolledUp, OMIM ID: 600361
HumanCMT2H619496Charcot-Marie-Tooth disease, axonal, type 2H
img HP RolledUp, OMIM ID: 607731
HumanLGMD1G553991limb girdle muscular dystrophy 1G (autosomal dominant)
img HP RolledUp, OMIM ID: 609115
HumanCMTDI2387574Charcot-Marie-Tooth disease, dominant intermediate 2
img HP RolledUp, OMIM ID: 606483
HumanLRSAM190678leucine rich repeat and sterile alpha motif containing 1
img HP RolledUp, OMIM ID: 614436
HumanSBF281846SET binding factor 2
img HP RolledUp, OMIM ID: 604563
HumanFA2H79152fatty acid 2-hydroxylase
img HP RolledUp, OMIM ID: 612319
HumanINF264423inverted formin, FH2 and WH2 domain containing
img HP RolledUp, OMIM ID: 614455
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 606071
HumanPRX57716periaxin
img HP RolledUp, OMIM ID: 145900
HumanGDAP154332ganglioside induced differentiation associated protein 1
img HP RolledUp, OMIM ID: 608340
HumanSMCHD123347structural maintenance of chromosomes flexible hinge domain containing 1
img HP RolledUp, OMIM ID: 158901
HumanKIF1B23095kinesin family member 1B
img HP RolledUp, OMIM ID: 118210
HumanMFN29927mitofusin 2
img HP RolledUp, OMIM ID: 609260
HumanTCAP8557titin-cap
img HP RolledUp, OMIM ID: 601954
HumanRAB7A7879RAB7A, member RAS oncogene family
img HP RolledUp, OMIM ID: 600882
HumanTTN7273titin
img HP RolledUp, OMIM ID: 603689
HumanPMP225376peripheral myelin protein 22
img HP RolledUp, OMIM ID: 145900
img HP RolledUp, OMIM ID: 118220
img HP RolledUp, OMIM ID: 118300
HumanNEFL4747neurofilament, light polypeptide
img HP RolledUp, OMIM ID: 607684
HumanMYH74625myosin, heavy chain 7, cardiac muscle, beta
img HP RolledUp, OMIM ID: 160500
HumanMPZ4359myelin protein zero
img HP RolledUp, OMIM ID: 607736
img HP RolledUp, OMIM ID: 145900
img HP RolledUp, OMIM ID: 118200
HumanMDRV4195muscular dystrophy, with rimmed vacuoles
img HP RolledUp, OMIM ID: 601846
HumanLMNA4000lamin A/C
img HP RolledUp, OMIM ID: 605588
HumanLBR3930lamin B receptor
img HP RolledUp, OMIM ID: 169400
HumanKARS3735lysyl-tRNA synthetase
img HP RolledUp, OMIM ID: 613641
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001436Abnormality of the foot musculature0self