Decreased serum copper
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
| Synonyms: |
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| Quality: | ||
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
MedDRA: |
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| Database Frequency: | 2 / 7739 | |
| Resource: |
All diseases associated with this symptom:
| Congenital cataract-hearing loss-severe developmental delay syndrome | (Orphanet:300313) |
| Occipital horn syndrome | (Orphanet:198) |