lysosomal storage disease with skeletal involvement
MONDO:0800088Mondo
Findings
No curated finding names lysosomal storage disease with skeletal involvement yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Where it sits
- A kind of
- Narrower terms (25)
- alpha-mannosidosis
- aspartylglucosaminuria
- beta-mannosidosis
- free sialic acid storage disease, infantile form
- fucosidosis
- galactosialidosis
- GM1 gangliosidosis type 1
- GNPTG-mucolipidosis
- Hurler syndrome
- Hurler-Scheie syndrome
- mucolipidosis type II
- mucolipidosis type III, alpha/beta
- mucopolysaccharidosis type 2
- mucopolysaccharidosis type 3A
- mucopolysaccharidosis type 3B
- mucopolysaccharidosis type 3C
- mucopolysaccharidosis type 3D
- mucopolysaccharidosis type 4A
- mucopolysaccharidosis type 4B
- mucopolysaccharidosis type 6
- mucopolysaccharidosis type 7
- mucopolysaccharidosis-plus syndrome
- mucosulfatidosis
- Scheie syndrome
- sialidosis type 2
Other names
1 name
Resolves to: lysosomal storage disease with skeletal involvement
- Also called
- dysostosis multiplex