Scleroderma-like changes
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 2 / 7739 | |
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All diseases associated with this symptom:
| Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
| Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |