Dysmyelination
Symptom Information:
| Symptom ID: | MedDRA:10067601 | ||
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HPO:
MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Metabolic and nutritional disorders congenital(MedDRA:10027424) Lysosomal storage disorders(MedDRA:10024579) Dysmyelination(MedDRA:10067601) |
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| Database Frequency: | 5 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
| COCKAYNE SYNDROME A | (OMIM:216400) |
| COCKAYNE SYNDROME B | (OMIM:133540) |
| Lethal encephalopathy due to mitochondrial and peroxisomal fission defect | (Orphanet:330050) |
| Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |