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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
mucolipidosis II alpha/beta
Summary
- Synonym
-
- I-cell disease
- inclusion-cell disease
- mucolipidosis II
- Definition
- A mucolipidosis that is characterized by short stature, skeletal abnormalities, cardiomegaly, and developmental delay, caused by a defect in proper lysosomal enzyme phosphorylation and localization, which results in accumulation of lysosomal substrates, and that has_material_basis_in homozygous or compound heterozygous mutation in the GNPTAB gene.
- Super Class
- mucolipidosis
External Links
- Disease Ontology
- DOID:0080070
- Mondo Disease Ontology
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002690 | Large sella turcica |
| HP:0002756 | Pathologic fracture |
| HP:0002804 | Arthrogryposis multiplex congenita |
| HP:0002837 | Recurrent bronchitis |
| HP:0002869 | Flared iliac wing |
| HP:0003016 | Metaphyseal widening |
| HP:0003026 | Short long bone |
| HP:0003180 | Flat acetabular roof |
| HP:0003264 | Deficiency of N-acetylglucosamine-1-phosphotransferase |
| HP:0003300 | Ovoid vertebral bodies |
