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Details
Link-It Detail - Human Phenotype - Abnormality of pelvic girdle bone morphology
Debug Stats
  • ### Total Build Time: 39 ms 34.420 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 219 bytes
  • CONCEPT_SOLR_HIT_STATS gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 799 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 6.859 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.112 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 23.271 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of pelvic girdle bone morphology HP:0002644
Parents (2)
img Abnormality of the skeletal system HP:0000924
img Abnormal appendicular skeleton morphology HP:0011844
Children (21)
img Coxa valga HP:0002673
img Abnormality of the ischium HP:0003174
img Coxa vara HP:0002812
img Abnormality of the ilium HP:0002867
img Small pelvis HP:0003373
img Abnormality of the greater sacrosciatic notch HP:0010456
img Abnormal pelvis bone ossification HP:0009106
img Abnormality of the coccyx HP:0008519
img Narrow pelvis HP:0003275
img Abnormality of the musculature of the pelvis HP:0001469
img Pelvic exostoses HP:0003276
img Abnormality of the hip bone HP:0003272
img Halberd-shaped pelvis HP:0002826
img Delayed proximal femoral epiphyseal ossification HP:0008828
img Square pelvis HP:0003278
img Abnormality of the pubic bones HP:0003172
img Limited hip movement HP:0008800
img Pelvic asymmetry HP:0010453
img Aplasia/Hypoplasia involving the pelvis HP:0009103
img Early ossification of capital femoral epiphyses HP:0008797
img Large pelvis HP:0010779
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the skeletal system HP:0000924
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal appendicular skeleton morphology HP:0011844
Genes (318)

Species:
human : 318
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCPBHM100820762Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
img HP TAS, OMIM ID: 300863
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDUP17Q23.1Q23.2100526743
img HP RolledUp, OMIM ID: 613618
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDUP17P13.3100379203
img HP RolledUp, OMIM ID: 613215
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP RolledUp, OMIM ID: 612475
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
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
HumanLGMD1G553991limb girdle muscular dystrophy 1G (autosomal dominant)
img HP RolledUp, OMIM ID: 609115
HumanLRSL406214Larsen-like syndrome
img HP RolledUp, OMIM ID: 608545
HumanLGMD1F404679limb girdle muscular dystrophy 1F (autosomal dominant)
img HP RolledUp, OMIM ID: 608423
HumanIFITM5387733interferon induced transmembrane protein 5
img HP IEA, OMIM ID: 610967
HumanACF387569Asymmetric crying facies (Cayler cardiofacial syndrome)
img HP RolledUp, OMIM ID: 125520
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP TAS, OMIM ID: 219000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002644Abnormality of pelvic girdle bone morphology0self