Neurology · Neurology / Metabolic disease
Mucopolysaccharidosis type II with neurological involvement
also: Hunter syndrome
X-linked lysosomal storage disease.
- Specialty
- Neurology
- Subspecialty
- Neurology / Metabolic disease
- Sex & age distribution
- Male: affected, nearly all; Female: carriers rarely affected; Children: yes, early childhood
- Gene(s) involved
- IDS
- Alternative names & eponyms
- Hunter syndrome
Etiology & mechanism
IDS mutation.
Gene(s) involved (1)
Symptoms & signs (4)
In plain terms, someone with Mucopolysaccharidosis type II with neurological involvement may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Hunter syndrome
hearing loss, hepatosplenomegaly
2 shared
Hurler syndrome
hearing loss, hepatosplenomegaly
2 shared
Mucopolysaccharidosis type I with neurological involvement
coarse features, cognitive decline
1 shared
Alport syndrome with diffuse leiomyomatosis
hearing loss
1 shared
Alström syndrome
hearing loss
1 shared
Branchio-oto-renal syndrome
hearing loss
1 shared
CARASIL
cognitive decline
1 shared
Chanarin–Dorfman syndrome
hearing loss
1 shared
CHARGE syndrome
hearing loss
1 shared
Cockayne syndrome
hearing loss
Shares genes with
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