Lysosomal amino acid transport disorder is a genetic condition affecting the transport of amino acids within lysosomes, leading to their accumulation and causing neurological issues, developmental delays, and metabolic problems.

Sialic acid metabolism disorder is a genetic condition affecting the breakdown or transport of sialic acid, leading to its accumulation in cells and causing neurological issues, developmental delays, and motor dysfunctions.

Glycoproteinosis is a group of rare lysosomal disorders affecting the breakdown of glycoproteins, leading to their accumulation in cells and causing neurological issues, developmental delays, and organ dysfunctions.

Lysosomal acid phosphatase deficiency is a rare genetic disorder causing the accumulation of fats and substances in cells due to impaired breakdown, leading to liver and spleen enlargement, neurological issues, and metabolic disorders.

Lysosomal glycogen storage disease is a rare genetic disorder caused by impaired glycogen breakdown within lysosomes, leading to its accumulation in cells and resulting in muscle weakness, heart and liver complications, and growth abnormalities.

Mucopolysaccharidosis (MPS) is a group of inherited lysosomal disorders affecting the breakdown of glycosaminoglycans, leading to their accumulation in cells and causing growth abnormalities, skeletal issues, heart problems, and neurological impairments.