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Details
Link-It Detail - Human Phenotype - Abnormality of the cerebrum
Debug Stats
  • ### Total Build Time: 67 ms 35.983 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 241 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
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 793 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 7.252 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 3.037 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 23.321 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cerebrum HP:0002060
Definition (1)
An abnormality of the `telencephalon` (FMA:62000), which is also known as the cerebrum.
Parents (2)
img Abnormality of the central nervous system HP:0002011
img Abnormality of the forebrain HP:0100547
Children (22)
img Cerebral calcification HP:0002514
img Cerebral edema HP:0002181
img Atrophy/Degeneration affecting the cerebrum HP:0007369
img Abnormality of the caudate nucleus HP:0002339
img Aplasia/Hypoplasia of the cerebrum HP:0007364
img Porencephaly HP:0002132
img Limbic malformations HP:0007343
img Cerebral arteriovenous malformation HP:0002408
img Primitive reflexes (palmomental, snout, glabellar) HP:0002476
img Abnormality of the cerebral white matter HP:0002500
img Granulovacuolar degeneration HP:0002528
img Abnormality of the cerebral subcortex HP:0010993
img Cerebral granulomatosis HP:0100313
img Cerebral inclusion bodies HP:0100314
img Diffuse cerebral sclerosis HP:0006918
img Leukoencephalopathy HP:0002352
img Schizencephaly HP:0010636
img Abnormality of the basal ganglia HP:0002134
img Abnormality of the cerebral cortex HP:0002538
img Abnormality of the corpus callosum HP:0001273
img Abnormality of the septum pellucidum HP:0007375
img Holoprosencephaly HP:0001360
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the forebrain HP:0100547
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the forebrain HP:0100547
Genes (850)

Species:
human : 850
Page Size
Current 25
  Page 1 of 34
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanCCCSX100820758Cerebral-cerebellar-coloboma syndrome, X-linked
img HP RolledUp, OMIM ID: 300864
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanMRT17100689013mental retardation, non-syndromic, autosomal recessive, 17
img HP RolledUp, OMIM ID: 614207
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL7Q11.23100653380
img HP RolledUp, OMIM ID: 613729
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
img HP RolledUp, OMIM ID: 612530
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanFWS100529224Forsythe-Wakeling syndrome
img HP RolledUp, OMIM ID: 613606
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanRJBS100528027Rajab syndrome
img HP RolledUp, OMIM ID: 613658
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002060Abnormality of the cerebrum0self