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Details
Link-It Detail - Human Phenotype - Abnormality of the mastoid
Debug Stats
  • ### Total Build Time: 12 ms 8.101 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 316 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=3 ms Completed: 3 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.105 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=4 ms Completed: 4 ms rowSize= 2.805 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the mastoid HP:0000264
Definition (1)
An abnormality of the `mastoid process` (FMA:52872), which is the conical prominence projecting from the undersurface of the mastoid portion of the temporal bone.
Parents (1)
img Abnormality of the skull HP:0000929
Children (3)
img Mastoiditis HP:0000265
img Delayed pneumatization of the mastoid process HP:0005906
img Advanced pneumatization of the mastoid process HP:0010724
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 (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanRAG25897recombination activating gene 2
img HP RolledUp, OMIM ID: 601457
HumanRAG15896recombination activating gene 1
img HP RolledUp, OMIM ID: 601457
HumanNBN4683nibrin
img HP RolledUp, OMIM ID: 251260
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000264Abnormality of the mastoid0self