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GATACA
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Details
Link-It Detail - Human Phenotype - Abnormality of the arachnoid mater
Debug Stats
  • ### Total Build Time: 23 ms 10.515 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= 205 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=5 ms Completed: 5 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 437 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.092 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 5.981 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the arachnoid mater HP:0100700
Definition (1)
An abnormality of the `Arachnoid mater` (FMA:9591).
Parents (1)
img Abnormality of the meninges HP:0010651
Children (1)
img Arachnoid cyst HP:0100702
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the meninges HP:0010651
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the meninges HP:0010651
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 600176
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanXPNPEP363929X-prolyl aminopeptidase (aminopeptidase P) 3, putative
img HP RolledUp, OMIM ID: 613159
HumanGPSM229899G-protein signaling modulator 2
img HP RolledUp, OMIM ID: 604213
HumanOFD18481oral-facial-digital syndrome 1
img HP RolledUp, OMIM ID: 311200
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
img HP RolledUp, OMIM ID: 153400
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 101200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100700Abnormality of the arachnoid mater0self