Decreased serum ceruloplasmin
Symptom Information:
| Symptom ID: | HPO:0010837 | ||
| Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of ion homeostasis(HPO:0003111) Abnormality of cation homeostasis(HPO:0010929) Abnormality of transition element cation homeostasis(HPO:0011030) Abnormality of copper homeostasis(HPO:0010836) Decreased serum ceruloplasmin(HPO:0010837) 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) |
| Wilson disease | (Orphanet:905) |