"Mucolipidoses" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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 |
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
- Cherry Red Spot-Myoclonus Syndrome
- Myoclonus-Cherry Red Spot Syndrome
- Mucolipidosis Type I
- Mucolipidosis I
- Cherry Red Spot Myoclonus Syndrome
- Myoclonus Cherry Red Spot Syndrome
- Mucolipidosis Type 1
Type III Mucolipidosis- Type III Mucolipidosis
- Mucolipidoses, Type III
- Mucolipidosis, Type III
- Type III Mucolipidoses
- Mucolipidosis III
- Pseudo-Hurler Polydystrophy
- Polydystrophy, Pseudo-Hurler
- Pseudo Hurler Polydystrophy
- Mucolipidosis IIIa
- Mucolipidosis III Alpha Beta
- Mucolipidosis Type III
- Psuedo-Hurler Disease
- Psuedo Hurler Disease
- Psuedo-Hurler Diseases
Type IV Mucolipidosis- Type IV Mucolipidosis
- Mucolipidoses, Type IV
- Mucolipidosis, Type IV
- Type IV Mucolipidoses
- Deficiency Disease, Ganglioside Sialidase
- Ganglioside Sialidase Deficiency Disease
- Sialolipidosis
- Sialolipidoses
- Mucolipidosis Type IV
- Mucolipidosis IV
Type II Mucolipidosis- Type II Mucolipidosis
- Mucolipidoses, Type II
- Mucolipidosis, Type II
- Type II Mucolipidoses
- I-Cell Disease
- I Cell Disease
- I-Cell Diseases
- Mucolipidosis Type II
- Inclusion Cell Disease
- Inclusion Cell Diseases
- Mucolipidosis II
|
Below are MeSH descriptors whose meaning is more general than "Mucolipidoses".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Metabolic [C05.116.198]
- Mucolipidoses [C05.116.198.371]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
- Mucolipidoses [C10.228.140.163.100.435.590]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
- Mucolipidoses [C16.320.565.189.435.590]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Mucolipidoses [C16.320.565.202.670]
- Lysosomal Storage Diseases [C16.320.565.595]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
- Mucolipidoses [C16.320.565.595.554.590]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
- Mucolipidoses [C18.452.132.100.435.590]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
- Mucolipidoses [C18.452.648.189.435.590]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Mucolipidoses [C18.452.648.202.670]
- Lysosomal Storage Diseases [C18.452.648.595]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
- Mucolipidoses [C18.452.648.595.554.590]
Below are MeSH descriptors whose meaning is more specific than "Mucolipidoses".
This graph shows the total number of publications written about "Mucolipidoses" by people in this website by year, and whether "Mucolipidoses" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Mucolipidoses" by people in Profiles.
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Cardiovascular involvement in alpha-n-acetyl neuraminidase deficiency syndromes (sialidosis type I and II). Cardiol Young. 2021 May; 31(5):862-864.
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Mucolipidosis Type II Affecting 1 Fetus and Placental Disk of a Dichorionic-Diamnionic Twin Gestation: A Case Report and Review of the Literature. Int J Gynecol Pathol. 2019 Jul; 38(4):346-352.
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Mucolipidosis type IV: clinical manifestations and natural history. Am J Med Genet. 1991 Dec 01; 41(3):313-8.