Abnormality of copper homeostasis
Symptom Information:
Symptom ID: | HPO:0010836 | ||||||
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) MedDRA: |
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Database Frequency: | 2 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Wilson disease | (Orphanet:905) |