Lysosomal storage disease with skeletal involvement

rare

Subtypes

Disease	ID	Subtypes	Genes
Alpha-mannosidosis	MONDO:0009561	3	MAN2B1
Mucopolysaccharidosis type 2	MONDO:0010674	2	IDS
Mucopolysaccharidosis type 6	MONDO:0009661	2	ARSB
Sialidosis type 2	MONDO:0009738	2	NEU1
GM1 gangliosidosis type 1	MONDO:0009260
GNPTG-mucolipidosis	MONDO:0009652		GNPTG
Hurler syndrome	MONDO:0011758		IDUA
Hurler-Scheie syndrome	MONDO:0011759		IDUA
Scheie syndrome	MONDO:0011760		IDUA
Aspartylglucosaminuria	MONDO:0008830		AGA
Beta-mannosidosis	MONDO:0009562		MANBA
Free sialic acid storage disease, infantile form	MONDO:0010027		SLC17A5
Fucosidosis	MONDO:0009254		FUCA1
Galactosialidosis	MONDO:0009737		CTSA
Mucolipidosis type II	MONDO:0009650
Mucolipidosis type III, alpha/beta	MONDO:0018931
Mucopolysaccharidosis type 3A	MONDO:0009655		SGSH
Mucopolysaccharidosis type 3B	MONDO:0009656		NAGLU
Mucopolysaccharidosis type 3C	MONDO:0009657		HGSNAT
Mucopolysaccharidosis type 3D	MONDO:0009658		GNS
Mucopolysaccharidosis type 4A	MONDO:0009659		GALNS
Mucopolysaccharidosis type 4B	MONDO:0009660		GLB1
Mucopolysaccharidosis type 7	MONDO:0009662		GUSB
Mucopolysaccharidosis-plus syndrome	MONDO:0015012		VPS33A
Mucosulfatidosis	MONDO:0010088		SUMF1

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