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MIRAGE
combined saposin deficiency
Summary
- Synonym
-
- PSAPD
- combined SAP deficiency
- encephalopathy due to prosaposin deficiency
- Definition
- A sphingolipidosis characterized by absence of expression of both isoforms of PSAP (SAP1 and SAP2) resulting in hepatosplenomegaly and severe neurological disease that has_material_basis_in homozygous or compound heterozygous mutation in PSAP on 10q22.1.
- Super Class
- sphingolipidosis
External Links
- Disease Ontology
- DOID:0111330
- Mondo Disease Ontology
- MeSH
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P07602 | Prosaposin |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q61207 | Prosaposin |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003487 | Babinski sign |
| HP:0000648 | Optic atrophy |
| HP:0002518 | Abnormal periventricular white matter morphology |
| HP:0003623 | Neonatal onset |
