ORPHA:309288
Alpha-mannosidosis, adult form
Also called Lysosomal alpha-D-mannosidase deficiency, adult form
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adult
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:309288 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Intellectual disability, mild
- Oligosacchariduria
- Ataxia
- Recurrent infections
- Asthenia
- Macroglossia