Functional motor problems
Symptom Information:
Symptom ID: | HPO:0004302 | ||
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 the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Functional motor problems(HPO:0004302) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |