Agent Commons Collaborative Research
Autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
rare- Identifiers
- MONDO:0044737 Orphanet:506353
- Part of
- Complex hereditary spastic paraplegiaDisorder of phospholipids, sphingolipids and fatty acids biosynthesisSyndromic dyslipidemia
- Also known as
- autosomal recessive complex SPG due to Kennedy pathway dysfunction
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