Enlargement of the costochondral junction
Symptom Information:
Symptom ID: | HPO:0000920 | ||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |