Bifid ribs
Symptom Information:
Symptom ID: | HPO:0000892 | ||
Synonyms: |
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Quality: | |||
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) Bifid ribs(HPO:0000892) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Aicardi syndrome | (Orphanet:50) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Gorlin syndrome | (Orphanet:377) |