Enlargement of the costochondral junction

Symptom Information:

Symptom ID: HPO:0000920
Synonyms:
Costochondral thickening [HPO:0000920]
Enlarged costochondral junctions [HPO:0000920]
Prominent costochondral junction [HPO:0000920]
Wide costochondral junctions [HPO:0000920]
Widened costochondral junction [HPO:0000920]
Costochondral thickening [OMIM:Costochondral thickening]
Enlargement of the costochondral junction [OMIM:Enlargement of the costochondral junction]
Prominent costochondral junction [OMIM:Prominent costochondral junction]
Wide costochondral junctions [OMIM:Wide costochondral junctions]
Widened costochondral junction [OMIM:Widened costochondral junction]
Quality:
Cross references:
OMIM: "Costochondral thickening" [OMIM:Costochondral thickening]
OMIM: "Enlargement of the costochondral junction" [OMIM:Enlargement of the costochondral junction]
OMIM: "Prominent costochondral junction" [OMIM:Prominent costochondral junction]
OMIM: "Wide costochondral junctions" [OMIM:Wide costochondral junctions]
OMIM: "Widened costochondral junction" [OMIM:Widened costochondral junction]
Is a (Direct Parents):
HPO         Abnormality of the costochondral junction
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the rib cage(HPO:0001547)
                      Abnormality of the ribs(HPO:0000772)
                         Abnormality of the costochondral junction(HPO:0000919)
                            Enlargement of the costochondral junction(HPO:0000920)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Multiple synostoses syndrome (Orphanet:3237)
Shwachman-Diamond syndrome (Orphanet:811)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B (OMIM:600081)