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Details
Link-It Detail - Human Phenotype - Abnormality of the costochondral junction
Debug Stats
  • ### Total Build Time: 44 ms 19.285 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 216 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 386 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=5 ms Completed: 5 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 3.401 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 3.010 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 10.673 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.035 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the costochondral junction HP:0000919
Definition (1)
Any anomaly of the `costochondral junction` (FMA:7956). The costochondral junctions are located between the distal part of the ribs and the costal cartilages, which are bars of hyaline cartilage that connect the ribs to the sternum.
Parents (1)
img Abnormality of the ribs HP:0000772
Children (10)
img Progressive calcification of costochondral cartilage HP:0006600
img Enlargement of the costochondral junction HP:0000920
img Rachitic rosary HP:0000897
img Costochondral joint sclerosis HP:0006623
img Irregular costochondral margins HP:0006658
img Bulging of the costochondral junction HP:0000893
img Precocious costochondral ossification HP:0006607
img Wide-cupped costochondral junctions HP:0000910
img Costochondral pain HP:0006649
img Irregular chondrocostal junctions HP:0006606
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the ribs HP:0000772
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the ribs HP:0000772
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the ribs HP:0000772
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
img HP RolledUp, OMIM ID: 612089
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img HP RolledUp, OMIM ID: 241530
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
img HP RolledUp, OMIM ID: 600081
HumanDYM54808dymeclin
img HP RolledUp, OMIM ID: 223800
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanNOG9241noggin
img HP RolledUp, OMIM ID: 186500
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanDDR24921discoidin domain receptor tyrosine kinase 2
img HP RolledUp, OMIM ID: 271665
HumanFGFR32261fibroblast growth factor receptor 3
img HP RolledUp, OMIM ID: 187601
img HP RolledUp, OMIM ID: 187600
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
img HP RolledUp, OMIM ID: 264700
HumanCTNS1497cystinosin, lysosomal cystine transporter
img HP RolledUp, OMIM ID: 219800
HumanALPL249alkaline phosphatase, liver/bone/kidney
img HP RolledUp, OMIM ID: 241500
img HP RolledUp, OMIM ID: 241510
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000919Abnormality of the costochondral junction0self