Cellular metachromasia
Symptom Information:
| Symptom ID: | HPO:0003653 | ||
| 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 carbohydrate metabolism/homeostasis(HPO:0011013) Abnormality of polysaccharide metabolism(HPO:0011012) Abnormality of glycosaminoglycan metabolism(HPO:0004371) Abnormality of mucopolysaccharide metabolism(HPO:0011020) Cellular metachromasia(HPO:0003653) MedDRA: |
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| Database Frequency: | 2 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Sanfilippo syndrome type C | (Orphanet:79271) |
| Sanfilippo syndrome type D | (Orphanet:79272) |