Fibroblast metachromasia
Symptom Information:
Symptom ID: | HPO:0003610 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) Fibroblast metachromasia(HPO:0003610) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
MORQUIO SYNDROME C | (OMIM:252300) |
MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES | (OMIM:252700) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |