hereditary spastic paraplegia 39
This syndrome is characterised by progressive spastic paraplegia and distal muscle wasting
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Summary
hereditary spastic paraplegia 39 is a rare disease[1]. It is known by 11 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: hereditary spastic paraplegia[4], autosomal recessive complex spastic paraplegia[5], disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement[6], syndromic dyslipidemia[7], autosomal recessive disease[8]
- Health specialty: neurology[9]
- Genetic association: PNPLA6[10]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110790[11], http://identifiers.org/doid/DOID:0110790[12], http://www.orpha.net/ORDO/Orphanet_139480[13]
- On focus list of Wikimedia project: WikiProject Medicine[14]