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Details
Link-It Detail - Human Phenotype - Abnormality of the corpus callosum
Debug Stats
  • ### Total Build Time: 57 ms 35.528 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 203 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 791 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.401 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 6.790 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 22.989 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.028 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of the corpus callosum HP:0001273
Definition (1)
Abnormality of the `corpus callosum` (FMA:86464).
Parents (2)
img Abnormality of the cerebrum HP:0002060
img Abnormality of the cerebral white matter HP:0002500
Children (10)
img Abnormal length of corpus callosum HP:0200011
img Atrophy/Degeneration of the corpus callosum HP:0007371
img Aplasia/Hypoplasia of the corpus callosum HP:0007370
img Dysgenesis of corpus callosum HP:0006996
img Abnormal thickness of corpus callosum HP:0200010
img Lipoma of corpus callosum HP:0006931
img Thick corpus callosum HP:0007074
img Dysplastic corpus callosum HP:0006989
img MRI shows defects of the corpus callosum HP:0007323
img Abnormal size of corpus callosum HP:0200009
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the cerebral white matter HP:0002500
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the cerebral white matter HP:0002500
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the cerebral white matter HP:0002500
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the cerebral white matter HP:0002500
Genes (246)

Species:
human : 246
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SpeciesGeneGeneIdGene NameEvidence
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanCCCSX100820758Cerebral-cerebellar-coloboma syndrome, X-linked
img HP RolledUp, OMIM ID: 300864
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDUP17P13.3100379203
img HP RolledUp, OMIM ID: 613215
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP RolledUp, OMIM ID: 612475
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanDEL1Q42Q44100190984Chromosome 1q42-q44 deletion syndrome
img HP RolledUp, OMIM ID: 612337
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanCHMRQ780925Cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
img HP RolledUp, OMIM ID: 610185
HumanISPD729920isoprenoid synthase domain containing
img HP RolledUp, OMIM ID: 614643
HumanSPG32724107spastic paraplegia 32 (autosomal recessive)
img HP RolledUp, OMIM ID: 611252
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001273Abnormality of the corpus callosum0self