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Details
Link-It Detail - Human Phenotype - Abnormality of the hip bone
Debug Stats
  • ### Total Build Time: 25 ms 34.129 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 199 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=0 Completed: 0 ms rowSize= 812 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 4.866 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.963 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 21.949 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 hip bone HP:0003272
Definition (1)
An abnormality of the `hip bone` (FMA:16585).
Parents (2)
img Abnormality of pelvic girdle bone morphology HP:0002644
img Abnormality of the joints of the lower limbs HP:0100491
Children (15)
img Coxa valga HP:0002673
img Coxa plana HP:0003280
img Hip dysplasia HP:0001385
img Abnormality of the ischium HP:0003174
img Coxa vara HP:0002812
img Decreased hip abduction HP:0003184
img Coxa magna HP:0003279
img Hip dislocation HP:0002827
img Abnormality of the ilium HP:0002867
img Abnormality of the acetabulum HP:0003170
img Abnormality of the hip joint HP:0001384
img Hip contracture HP:0003273
img Abnormality of the pubic bones HP:0003172
img Arthralgia of the hip HP:0003365
img Abnormality of the femoral neck and head region HP:0003366
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of pelvic girdle bone morphology HP:0002644
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of pelvic girdle bone morphology HP:0002644
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the joints of the lower limbs HP:0100491
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the joints of the lower limbs HP:0100491
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the joints of the lower limbs HP:0100491
Genes (263)

Species:
human : 263
Page Size
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCPBHM100820762Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
HumanDEL2Q23.1100820633
img HP TAS, OMIM ID: 156200
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDUP17Q23.1Q23.2100526743
img HP TAS, OMIM ID: 613618
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL17Q23.1Q23.2100415941
img HP TAS, OMIM ID: 613355
HumanDUP17P13.3100379203
img HP TAS, OMIM ID: 613215
HumanDEL19Q13.11100306978
img HP TAS, OMIM ID: 613026
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP TAS, OMIM ID: 612475
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP TAS, OMIM ID: 611867
HumanCFSS100188773craniofacioskeletal syndrome
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanACTD780896Acetabular dysplasia
img HP RolledUp, OMIM ID: 142700
HumanAMCX5619510arthrogryposis, X-linked, type 5
img HP RolledUp, OMIM ID: 300158
HumanLRSL406214Larsen-like syndrome
img HP TAS, OMIM ID: 608545
HumanACF387569Asymmetric crying facies (Cayler cardiofacial syndrome)
img HP TAS, OMIM ID: 125520
HumanFREM2341640FRAS1 related extracellular matrix protein 2
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanARX170302aristaless related homeobox
img HP TAS, OMIM ID: 300004
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003272Abnormality of the hip bone0self