metachromatic leukodystrophy, adult form
MONDO:0017730Mondo
Findings
No curated finding names metachromatic leukodystrophy, adult form yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
48 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal glycosphingolipid metabolismHPOHP:0004343
- Frequent (30% to 79% of cases)
- Abnormal social behaviorHPOHP:0012433
- Frequent (30% to 79% of cases)
- ClumsinessHPOHP:0002312
- Frequent (30% to 79% of cases)
- Decreased nerve conduction velocityHPOHP:0000762
- Frequent (30% to 79% of cases)
- DelusionHPOHP:0000746
- Frequent (30% to 79% of cases)
- DementiaHPOHP:0000726
- Frequent (30% to 79% of cases)
- Developmental regressionHPOHP:0002376
- Frequent (30% to 79% of cases)
- DysarthriaHPOHP:0001260
- Frequent (30% to 79% of cases)
- DystoniaHPOHP:0001332
- Frequent (30% to 79% of cases)
- Emotional labilityHPOHP:0000712
- Frequent (30% to 79% of cases)
- Frequent fallsHPOHP:0002359
- Frequent (30% to 79% of cases)
- Gait disturbanceHPOHP:0001288
- Frequent (30% to 79% of cases)
Show the remaining 36
- Generalized hypotoniaHPOHP:0001290
- Frequent (30% to 79% of cases)
- HallucinationsHPOHP:0000738
- Frequent (30% to 79% of cases)
- HyporeflexiaHPOHP:0001265
- Frequent (30% to 79% of cases)
- Increased CSF protein concentrationHPOHP:0002922
- Frequent (30% to 79% of cases)
- LeukodystrophyHPOHP:0002415
- Frequent (30% to 79% of cases)
- Memory impairmentHPOHP:0002354
- Frequent (30% to 79% of cases)
Where it sits
Other names
2 names
Resolves to: metachromatic leukodystrophy, adult form
- Also called
- arylsulfatase A deficiency, adult formMLD, adult form