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Details
Link-It Detail - Human Phenotype - Abnormality of neuronal migration
Debug Stats
  • ### Total Build Time: 22 ms 26.070 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 318 bytes
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  • Reload Stats
Human Phenotype (1)
Abnormality of neuronal migration HP:0002269
Definition (1)
An abnormality resulting from an anomaly of neuronal migration, i.e., of the process by which neurons travel from their origin to their final position in the brain.
Parents (3)
img Heterotopias/abnormal migration HP:0007317
img Abnormality of the nervous system HP:0000707
img Morphological abnormality of the central nervous system HP:0007319
Children (2)
img Abnormal cortical gyration HP:0002536
img Heterotopia HP:0002282
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Heterotopias/abnormal migration HP:0007317
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the nervous system HP:0000707
img All HP:0000001img Phenotypic abnormality HP:00001186img Morphological abnormality of the central nervous system HP:0007319
Genes (142)

Species:
human : 142
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTET18P100750329Tetrasomy 18p
img HP TAS, OMIM ID: 614290
HumanOCLN100506658occludin
HumanDEL2P16.1-P15100240740
img HP TAS, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
HumanAOS100188340Adams-Oliver syndrome
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanISPD729920isoprenoid synthase domain containing
img HP RolledUp, OMIM ID: 614643
HumanTUBB2B347733tubulin, beta 2B class IIb
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanDOK7285489docking protein 7
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 604317
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
img HP RolledUp, OMIM ID: 608716
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP TAS, OMIM ID: 300215
HumanBMPER168667BMP binding endothelial regulator
HumanB3GALNT2148789beta-1,3-N-acetylgalactosaminyltransferase 2
img HP RolledUp, OMIM ID: 615181
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP TAS, OMIM ID: 235510
HumanTMEM6791147transmembrane protein 67
img HP TAS, OMIM ID: 216360
HumanTUBGCP685378tubulin, gamma complex associated protein 6
img HP TAS, OMIM ID: 251270
HumanPOMGNT284892protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
img HP RolledUp, OMIM ID: 614830
HumanCOL18A180781collagen, type XVIII, alpha 1
HumanFRAS180144Fraser syndrome 1
img HP RolledUp, OMIM ID: 219000
HumanDYNC2H179659dynein, cytoplasmic 2, heavy chain 1
HumanMCPH179648microcephalin 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002269Abnormality of neuronal migration0self