All diseases

OMIM ID
612319
OMIM term:
SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
Alternative terms:
FATTY ACID HYDROXYLASE-ASSOCIATED NEURODEGENERATION; FAHN
LEUKODYSTROPHY, DYSMYELINATING, AND SPASTIC PARAPARESIS WITH OR WITHOUT DYSTONIA
(∗) Location:
16q23.1  
(†) Associated OMIM genes:
FA2H  
(‡) Associated MGI genes:
Fa2h  

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