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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
neuronal ceroid lipofuscinosis 10
Summary
- Synonym
-
- CLN10
- Cathepsin D deficiency
- neuronal ceroid lipofuscinosis cathepsin D-deficient
- neuronal ceroid lipofuscinosis due to cathepsin D deficiency
- Definition
- A neuronal ceroid lipofuscinosis that has_material_basis_in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15.
- Super Class
- autosomal recessive disease neuronal ceroid lipofuscinosis
External Links
- Disease Ontology
- DOID:0110725
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75503 | Bis(monoacylglycero)phosphate synthase CLN5 | |
| P07602 | Prosaposin | |
| P09382 | Galectin-1 | |
| P50897 | Palmitoyl-protein thioesterase 1 | |
| P53396 | ATP-citrate synthase | |
| P98161 | Polycystin-1 | |
| Q96EG1 | Arylsulfatase G | |
| Q9UMR5 | Lysosomal thioesterase PPT2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011209 | EEG with generalized slow activity grade 4 |
| HP:0012379 | Abnormal circulating enzyme concentration or activity |
| HP:0000529 | Progressive visual loss |
| HP:0000543 | Optic disc pallor |
| HP:0000580 | Pigmentary retinopathy |
| HP:0000712 | Emotional lability |
| HP:0000716 | Depression |
| HP:0000975 | Hyperhidrosis |
| HP:0001129 | Large central visual field defect |
| HP:0001300 | Parkinsonism |
