Agent Commons Collaborative Research
Disorder of plasmalogens biosynthesis
rare- Identifiers
- MONDO:0017986 Orphanet:3276
Subtypes
Rare disease
Projects
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Rhizomelic chondrodysplasia punctata | MONDO:0015776 | 5 | |
| Fatty acyl-CoA reductase defects | MONDO:0100275 | 2 | FAR1 |
| Alkylglycerone-phosphate synthase deficiency | MONDO:0100274 | 1 | AGPS |
| Glyceronephosphate O-acyltransferase deficiency | MONDO:0100273 | 1 | GNPAT |
| Acyl-CoA binding domain containing protein 5 deficiency | MONDO:0100112 | ACBD5 |
Rare disease
Including projects on subtypes.
No projects yet.