Prominent heel
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
SMITH-MCCORT DYSPLASIA 2 | (OMIM:615222) |
Spondyloepiphyseal dysplasia, MacDermot type | (Orphanet:163668) |
THREE M SYNDROME 1 | (OMIM:273750) |
THREE M SYNDROME 3 | (OMIM:614205) |