alpha-mannosidosis, adult form
MONDO:0017733Mondo
Findings
No curated finding names alpha-mannosidosis, adult form yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
30 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.
- Mild intellectual disabilityHPOHP:0001256
- Very frequent (80% to 99% of cases)
- OligosacchariduriaHPOHP:0010471
- Very frequent (80% to 99% of cases)
- AstheniaHPOHP:0025406
- Frequent (30% to 79% of cases)
- AtaxiaHPOHP:0001251
- Frequent (30% to 79% of cases)
- Recurrent infectionsHPOHP:0002719
- Frequent (30% to 79% of cases)
- AnxietyHPOHP:0000739
- Occasional (5% to 29% of cases)
- Atypical behaviorHPOHP:0000708
- Occasional (5% to 29% of cases)
- CataractHPOHP:0000518
- Occasional (5% to 29% of cases)
- Cerebellar atrophyHPOHP:0001272
- Occasional (5% to 29% of cases)
- Cerebral cortical atrophyHPOHP:0002120
- Occasional (5% to 29% of cases)
- ClumsinessHPOHP:0002312
- Occasional (5% to 29% of cases)
- ConfusionHPOHP:0001289
- Occasional (5% to 29% of cases)
Show the remaining 18
- Delayed speech and language developmentHPOHP:0000750
- Occasional (5% to 29% of cases)
- DelusionHPOHP:0000746
- Occasional (5% to 29% of cases)
- DepressionHPOHP:0000716
- Occasional (5% to 29% of cases)
- DrowsinessHPOHP:0002329
- Occasional (5% to 29% of cases)
- HallucinationsHPOHP:0000738
- Occasional (5% to 29% of cases)
- HepatosplenomegalyHPOHP:0001433
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: alpha-mannosidosis, adult form
- Also called
- lysosomal alpha-D-mannosidase deficiency, adult form