ORPHA:79270

Sanfilippo syndrome type B

Also called MPS3B, MPSIIIB, Mucopolysaccharidosis type 3B, Mucopolysaccharidosis type IIIB, N-acetyl-alpha-glucosaminidase deficiency

Body system

Bone diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:79270 is classified under "Bone diseases" in the Orphanet nomenclature.