ORPHA:88616
Autosomal recessive non-syndromic intellectual disability
Also called AR-NSID, NS-ARID
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood, Infancy
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:88616 is classified under "Neurological diseases" in the Orphanet nomenclature.