Related Conditions and Treatments
Alpha-mannosidosis
Condition
Alpha-mannosidosis is a condition characterized by an inability to break down complex sugars in the body’s cells.
Batten Disease
Condition
Batten disease is a very rare genetic disorder that affects the brain and nervous system.
Beta-mannosidosis
Condition
Beta-mannosidosis is a very rare genetic condition that affects the way certain types of sugar molecules are processed by the body.
Danon Disease
Condition
Danon disease is a rare inherited disorder that affects many organ systems.
Fabry Disease
Condition
Fabry disease is a lysosomal storage disorder that is progressive in nature and affects many of the body’s systems.
Fucosidosis
Condition
Fucosidosis is a rare genetic condition characterized by an inability to properly break down certain sugars attached to specific proteins and fats in the body’s cells.
GM1 Gangliosidosis
Condition
GM1 gangliosidosis, also called beta-galactosidase-1 deficiency, is a genetic disorder that progressively destroys nerve cells in the brain and spinal cord.
GM2 Gangliosidosis
Condition
GM2 gangliosidosis is a rare genetic disorder that progressively destroys nerve cells in the brain and spinal cord.
Krabbe Disease
Condition
Krabbe disease is when an abnormal accumulation of fat molecules affects the cells in the nervous system.
Lysosomal Acid Lipase Deficiency
Condition
Lysosomal acid lipase deficiency is a subset of lysosomal acid lipase deficiency (LALD).
MPS I (Hurler Syndrome)
Condition
Children with mucopolysarcharidosis type I (MPS I) have an abnormal accumulation of complex sugars in their cells, which affects many of the systems in their bodies.
MPS II (Hunter Syndrome)
Condition
Children with mucopolysarcharidosis type II (MPS II) have an abnormal accumulation of complex sugars in their cells, which affects many systems in their bodies.
Mucolipidosis I (ML I)
Condition
Mucolipidosis I (ML I), or sialidosis, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mucolipidosis II (ML II)
Condition
Mucolipidosis II (ML II), or I-cell disease, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mucolipidosis III (ML III)
Condition
Mucolipidosis III (ML III) is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mucopolysarcharidosis Type IVB (MPS IVB)
Condition
Mucopolysarcharidosis type IVB (MPS IVB), also known as Morquio syndrome type B, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mucopolysarcharidosis Type VI (MPS VI)
Condition
Mucopolysarcharidosis type VI (MPS VI), also known as Maroteaux-Lamay syndrome, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Multiple Sulfatase Deficiency
Condition
Multiple sulfatase deficiency is a complex, inherited disorder caused by a genetic mutation.
Niemann-Pick Disease Type B
Condition
Niemann-Pick disease type B is a rare genetic condition that affects many of the body’s organs and systems, including the central nervous system.
Niemann-Pick Disease Type C
Condition
Niemann-Pick disease is a rare genetic condition that affects many of the body’s organs and systems, including the central nervous system.
Pompe Disease
Condition
Pompe disease is caused by a genetic mutation that causes a buildup of complex sugars in the body’s tissues.
Sanfilippo Syndrome
Condition
Sanfilippo syndrome (aka mucopolysaccharidosis type III (MPS III)) is a rare, inherited disorder that's classified as a lysosomal storage disorder (LSD).
Sialic Acid Storage Disease
Condition
Sialic acid storage disease is a rare, inherited disorder that predominantly affects the central nervous system.