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Details
Link-It Detail - Human Phenotype - Abnormality of the femoral neck
Debug Stats
  • ### Total Build Time: 36 ms 31.845 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 286 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= 468 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.996 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 4.979 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 22.762 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the femoral neck HP:0003367
Definition (1)
An abnormality of the `femoral neck` (FMA:42385) (which is the process of bone, connecting the femoral head with the femoral shaft).
Parents (1)
img Abnormality of the femoral neck and head region HP:0003366
Children (6)
img Coxa valga HP:0002673
img Coxa vara HP:0002812
img Narrow femoral neck HP:0008819
img Short femoral neck HP:0003032
img Broad femoral neck HP:0006429
img Hypoplasia of the femoral neck HP:0100864
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the femoral neck and head region HP:0003366
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the femoral neck and head region HP:0003366
img All HP:0000001img Phenotypic abnormality HP:000011811img Abnormality of the femoral neck and head region HP:0003366
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the femoral neck and head region HP:0003366
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the femoral neck and head region HP:0003366
Genes (63)

Species:
human : 63
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP17Q23.1Q23.2100526743
img HP RolledUp, OMIM ID: 613618
HumanB3GALT6126792UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
img HP RolledUp, OMIM ID: 271640
HumanCANT1124583calcium activated nucleotidase 1
img HP RolledUp, OMIM ID: 251450
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
img HP RolledUp, OMIM ID: 612350
HumanCTC180169CTS telomere maintenance complex component 1
img HP RolledUp, OMIM ID: 612199
HumanSIL164374SIL1 nucleotide exchange factor
img HP RolledUp, OMIM ID: 248800
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 277590
HumanFKBP1060681FK506 binding protein 10, 65 kDa
img HP RolledUp, OMIM ID: 610968
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 184252
img HP RolledUp, OMIM ID: 113500
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanRAB2351715RAB23, member RAS oncogene family
img HP RolledUp, OMIM ID: 201000
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanBRKS50963Telopeptide lysyl hydroxylase, bone-specific
img HP RolledUp, OMIM ID: 259450
HumanBFHD50947Beukes familial hip dysplasia
img HP RolledUp, OMIM ID: 142669
HumanOSTM128962osteopetrosis associated transmembrane protein 1
img HP RolledUp, OMIM ID: 259700
HumanPOC1A25886POC1 centriolar protein A
img HP RolledUp, OMIM ID: 614813
HumanORC623594origin recognition complex, subunit 6
img HP RolledUp, OMIM ID: 613803
HumanB4GALT711285xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
img HP RolledUp, OMIM ID: 130070
HumanCRTAP10491cartilage associated protein
img HP RolledUp, OMIM ID: 610682
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
img HP RolledUp, OMIM ID: 259700
HumanPRG410216proteoglycan 4
img HP RolledUp, OMIM ID: 208250
HumanABCC910060ATP-binding cassette, sub-family C (CFTR/MRP), member 9
img HP RolledUp, OMIM ID: 239850
HumanRBM8A9939RNA binding motif protein 8A
img HP RolledUp, OMIM ID: 274000
HumanIFT1409742intraflagellar transport 140 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 266920
HumanADAMTSL29719ADAMTS-like 2
img HP RolledUp, OMIM ID: 231050
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003367Abnormality of the femoral neck0self