A group of inherited metabolic diseases characterized by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. INTELLECTUAL DISABILITY and skeletal changes, most notably dysostosis multiplex, occur frequently. (From Joynt, Clinical Neurology, 1992, Ch56, pp36-7)

Descriptor ID	D009081
MeSH Number(s)	C05.116.198.371 C10.228.140.163.100.435.590 C16.320.565.189.435.590 C16.320.565.202.670 C16.320.565.595.554.590 C18.452.132.100.435.590 C18.452.648.189.435.590 C18.452.648.202.670 C18.452.648.595.554.590
Concept/Terms	Mucolipidoses Mucolipidoses Mucolipidosis Type IV Mucolipidosis Type IV Mucolipidosis Mucolipidoses, Type IV Mucolipidosis, Type IV Type IV Mucolipidoses Sialolipidosis Sialolipidoses Mucolipidosis IV Mucolipidosis Type IV Mucolipidosis Type IVs Deficiency Disease, Ganglioside Sialidase Ganglioside Sialidase Deficiency Disease Type II Mucolipidosis Type II Mucolipidosis Mucolipidoses, Type II Mucolipidosis, Type II Type II Mucolipidoses Mucolipidosis Type II Mucolipidosis II I-Cell Disease Disease, I-Cell Diseases, I-Cell I Cell Disease I-Cell Diseases Inclusion Cell Disease Cell Disease, Inclusion Cell Diseases, Inclusion Disease, Inclusion Cell Diseases, Inclusion Cell Inclusion Cell Diseases Type III Mucolipidosis Type III Mucolipidosis Mucolipidoses, Type III Mucolipidosis, Type III Type III Mucolipidoses Mucolipidosis III Mucolipidosis IIIs Psuedo-Hurler Disease Disease, Psuedo-Hurler Diseases, Psuedo-Hurler Psuedo Hurler Disease Psuedo-Hurler Diseases Mucolipidosis IIIa IIIa, Mucolipidosis Mucolipidosis Type III Pseudo-Hurler Polydystrophy Polydystrophy, Pseudo-Hurler Pseudo Hurler Polydystrophy Ml III Alpha/Beta Alpha/Beta, Ml III Mucolipidosis III Alpha/Beta Alpha/Beta, Mucolipidosis III Alpha/Betas, Mucolipidosis III III Alpha/Beta, Mucolipidosis III Alpha/Betas, Mucolipidosis Lipomucopolysaccharidosis Lipomucopolysaccharidosis Lipomucopolysaccharidoses Type I Mucolipidosis Type I Mucolipidosis Mucolipidoses, Type I Mucolipidosis, Type I Type I Mucolipidoses Glycoprotein Neuraminidase Deficiency Deficiencies, Glycoprotein Neuraminidase Deficiency, Glycoprotein Neuraminidase Glycoprotein Neuraminidase Deficiencies Neuraminidase Deficiencies, Glycoprotein Neuraminidase Deficiency, Glycoprotein Mucolipidosis I Mucolipidosis Is Myoclonus-Cherry Red Spot Syndrome Mucolipidosis Type I Mucolipidosis Type Is Myoclonus Cherry Red Spot Syndrome Sialidosis Sialidoses Cherry Red Spot-Myoclonus Syndrome Cherry Red Spot Myoclonus Syndrome Mucolipidosis Type 1 Mucolipidosis Type 1s

Below are MeSH descriptors whose meaning is more general than "Mucolipidoses".

Below are MeSH descriptors whose meaning is related to "Mucolipidoses".

Below are MeSH descriptors whose meaning is more specific than "Mucolipidoses".