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Details
Link-It Detail - Human Phenotype - Abnormality of the foramen magnum
Debug Stats
  • ### Total Build Time: 17 ms 11.883 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 270 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=4 ms Completed: 4 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.065 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.086 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 6.658 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the foramen magnum HP:0002699
Definition (1)
Any abnormality of the foramen magnum (the aperture through which the medulla oblongata enters and exits the skull).
Parents (1)
img Abnormality of the skull HP:0000929
Children (3)
img Large foramen magnum HP:0002700
img Small foramen magnum HP:0002677
img Foramen magnum lesion HP:0005758
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the skull HP:0000929
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the skull HP:0000929
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanRAB2351715RAB23, member RAS oncogene family
img HP RolledUp, OMIM ID: 201000
HumanGPSM229899G-protein signaling modulator 2
img HP RolledUp, OMIM ID: 604213
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 305620
HumanFGFR32261fibroblast growth factor receptor 3
img HP RolledUp, OMIM ID: 187600
img HP RolledUp, OMIM ID: 100800
img HP RolledUp, OMIM ID: 187601
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanRUNX2860runt-related transcription factor 2
img HP RolledUp, OMIM ID: 119600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002699Abnormality of the foramen magnum0self