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 Deficiency Disease, Ganglioside Sialidase Mucolipidosis IV Ganglioside Sialidase Deficiency Disease Mucolipidosis Type IV Mucolipidosis Type IVs Type II Mucolipidosis Type II Mucolipidosis Mucolipidoses, Type II Mucolipidosis, Type II Type II Mucolipidoses Mucolipidosis II Mucolipidosis Type II I-Cell Disease I Cell Disease I-Cell Diseases Inclusion Cell Disease Cell Disease, Inclusion Disease, Inclusion Cell Inclusion Cell Diseases Type III Mucolipidosis Type III Mucolipidosis Mucolipidoses, Type III Mucolipidosis, Type III Type III Mucolipidoses Pseudo-Hurler Polydystrophy Polydystrophy, Pseudo-Hurler Pseudo Hurler Polydystrophy Mucolipidosis IIIa Mucolipidosis III Mucolipidosis IIIs Psuedo-Hurler Disease Psuedo Hurler Disease Psuedo-Hurler Diseases Mucolipidosis III Alpha Beta Mucolipidosis Type III Lipomucopolysaccharidosis Lipomucopolysaccharidosis Lipomucopolysaccharidoses Type I Mucolipidosis Type I Mucolipidosis Mucolipidoses, Type I Mucolipidosis, Type I Type I Mucolipidoses Cherry Red Spot Myoclonus Syndrome Myoclonus Cherry Red Spot Syndrome Myoclonus-Cherry Red Spot Syndrome Sialidosis Sialidoses Mucolipidosis Type 1 Mucolipidosis Type 1s Glycoprotein Neuraminidase Deficiency Deficiencies, Glycoprotein Neuraminidase Deficiency, Glycoprotein Neuraminidase Glycoprotein Neuraminidase Deficiencies Neuraminidase Deficiencies, Glycoprotein Neuraminidase Deficiency, Glycoprotein Cherry Red Spot-Myoclonus Syndrome Mucolipidosis I Mucolipidosis Is Mucolipidosis Type I Mucolipidosis Type Is

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".