hereditary spastic paraplegia 35 ^{الإنجليزية} (Q5934873)

A hereditary spastic paraplegia that has material basis in mutation in the FA2H gene on chromosome 16q23.1. ^{الإنجليزية}

اللغة	التسمية	الوصف	أسماء أخرى
العربية	لم تُضف التسمية	لا يوجد وصف
الإنجليزية	hereditary spastic paraplegia 35	A hereditary spastic paraplegia that has material basis in mutation in the FA2H gene on chromosome 16q23.1.	FAHN leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia autosomal recessive spastic paraplegia type 35 autosomal recessive spastic paraplegia 35 fatty acid hydroxylase-associated neurodegeneration SPG35 SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE hereditary spastic paraplegia type 35 SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35 Leukodystrophy, Dysmyelinating, and Spastic Paraparesis With or Without Dystonia

بيانات

Wikidata item ^{الإنجليزية}

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