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mucopolysaccharidosis IVA
Summary
- Synonym
-
- GALNS deficiency
- MPS IVA
- MPS4A
- Morquio A disease
- Morquio syndrome A
- Definition
- A mucopolysaccharidosis IV characterized by intracellular accumulation of keratan sulfate and chondroitin-6-sulfate resulting in short stature, skeletal dysplasia, dental anomalies, and corneal clouding that has_material_basis_in homozygous or compound heterozygous mutation in the GALNS gene on chromosome 16q24.3.
- Super Class
- autosomal recessive disease mucopolysaccharidosis IV
External Links
- Disease Ontology
- DOID:0111391
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8NBK3 | Formylglycine-generating enzyme |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003016 | Metaphyseal widening |
| HP:0003049 | Ulnar deviation of the wrist |
| HP:0003053 | Epiphyseal deformities of tubular bones |
| HP:0003277 | Constricted iliac wing |
| HP:0003300 | Ovoid vertebral bodies |
| HP:0003307 | Hyperlordosis |
| HP:0003308 | Cervical subluxation |
| HP:0003311 | Hypoplasia of the odontoid process |
| HP:0003521 | Disproportionate short-trunk short stature |
| HP:0003593 | Infantile onset |
