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Kanzaki disease
Summary
- Synonym
-
- NAGA deficiency type 2
- adult-onset alpha-N-acetylgalactosaminidase deficiency
- alpha-N-acetylgalactosaminidase deficiency type 2
- Definition
- A Schindler disease characterized by adult-onset of angiokeratoma corporis diffusum and mild intellectual impairment that has_material_basis_in homozygous mutation in the gene encoding alpha-N-galactosaminidase (NAGA) on chromosome 22q13.
- Super Class
- Schindler disease
External Links
- Disease Ontology
- DOID:0112319
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P17050 | Alpha-N-acetylgalactosaminidase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000365 | Hearing impairment |
| HP:0000962 | Hyperkeratosis |
| HP:0000214 | Lip telangiectasia |
| HP:0001004 | Lymphedema |
| HP:0000360 | Tinnitus |
| HP:0000280 | Coarse facial features |
| HP:0000503 | Tortuosity of conjunctival vessels |
| HP:0000179 | Thick lower lip vermilion |
| HP:0000967 | Petechiae |
| HP:0000958 | Dry skin |
