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Details
Link-It Detail - Human Phenotype - Abnormal trabecular bone morphology
Debug Stats
  • ### Total Build Time: 17 ms 20.314 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 782 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 772 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.896 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 12.313 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal trabecular bone morphology HP:0100671
Definition (1)
Abnormal structure or form of `trabecular bone` (FMA:24019).
Parents (2)
img Abnormality of bone mineral density HP:0004348
img Abnormal bone structure HP:0003330
Children (2)
img Rough bone trabeculation HP:0100670
img Sparse bone trabeculae HP:0002752
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of bone mineral density HP:0004348
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of bone mineral density HP:0004348
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of bone mineral density HP:0004348
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal bone structure HP:0003330
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormal bone structure HP:0003330
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img HP RolledUp, OMIM ID: 241530
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
img HP RolledUp, OMIM ID: 600081
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 156530
img HP RolledUp, OMIM ID: 168400
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 275210
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
img HP PCS, OMIM ID: 612301
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
img HP RolledUp, OMIM ID: 239000
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img HP RolledUp, OMIM ID: 300009
HumanLMNA4000lamin A/C
img HP RolledUp, OMIM ID: 275210
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
img HP RolledUp, OMIM ID: 264700
HumanCLCN51184chloride channel, voltage-sensitive 5
img HP RolledUp, OMIM ID: 300554
img HP RolledUp, OMIM ID: 300009
HumanACP554acid phosphatase 5, tartrate resistant
img HP RolledUp, OMIM ID: 607944
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100671Abnormal trabecular bone morphology0self