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Diseases
Genes (844)
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LIPA
Acid Lipase Disease
Lysosomal Acid Lipase Deficiency
Cholesteryl Ester Storage Disease
Niemann–pick Disease, Type C
Lysosomal Storage Disease
GAA
Glycogen Storage Disease Due To Acid Maltase Deficiency, Infantile Onset
Glycogen Storage Disease Due To Acid Maltase Deficiency, Late-Onset
Lysosomal Storage Disease
Glycogen Storage Disease Type 2
Glycogen Storage Disease Type 4
SLC17A5
Salla Disease
Free Sialic Acid Storage Disease
Infantile Free Sialic Acid Storage Disease
Lysosomal Storage Disease
Glycogen Storage Disease Type 2
GBE1
Glycogen Storage Disease Type Iii
Glycogen Storage Disease Type 2
Glycogen Storage Disease Type 4
GNE
Salla Disease
Free Sialic Acid Storage Disease
PYGM
Glycogen Storage Disease Type V
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
NPC1
Lipid Storage Disorder
Niemann–pick Disease, Type C
Lysosomal Storage Disease
F12
Factor Xii Deficiency
ABHD5
Neutral Lipid Storage Disease With Myopathy
Neutral Lipid Storage Disease
FOXP3
Ipex Syndrome
Niemann–pick Disease, Type C
AGL
Glycogen Storage Disease Type Iii
Glycogen Storage Disease Type 2
PNPLA2
Neutral Lipid Storage Disease With Myopathy
Glycogen Storage Disease Type 2
Neutral Lipid Storage Disease
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
G6PC
Glycogen Storage Disease Type Ix
Glycogen Storage Disease Type 1a
Glycogen Storage Disease Type Iii
Glycogen Storage Disease Type 2
Glycogen Storage Disease Type 4
MYH7
Myosin Storage Myopathy
GYS2
Orofaciodigital Syndrome 1
Glycogen Storage Disease Type 0
Glycogen Storage Disease Type 0, Liver
Glycogen Storage Disease Type Iii
PRPS1
Arts Syndrome
UBA1
X-Linked Spinal Muscular Atrophy Type 2
PYGL
Glycogen Storage Disease Type Ix
Glycogen Storage Disease Type V
Glycogen Storage Disease Type Iii
Glycogen Storage Disease Vi