Porphyrinuria
Symptom Information:
| Symptom ID: | HPO:0010473 | ||||
| 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 the heme biosynthetic pathway(HPO:0010472) Porphyrinuria(HPO:0010473) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Metabolic and nutritional disorders congenital(MedDRA:10027424) Inborn errors of porphyrin metabolism(MedDRA:10021607) Porphyrinuria(HPO:0010473) |
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| Database Frequency: | 2 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Porphyria cutanea tarda | (Orphanet:101330) |
| Porphyria variegata | (Orphanet:79473) |