Human Disease and Mouse Model Detail
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Human Disease
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Spastic Paraplegia 35, Autosomal Recessive; SPG35
OMIM ID: 612319
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Synonyms
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Fatty Acid Hydroxylase-Associated Neurodegeneration; FAHN;
Leukodystrophy, Dysmyelinating, and Spastic Paraparesis with or without Dystonia
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Fa2h*
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FA2H*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Spastic Paraplegia 35, Autosomal Recessive; SPG35
Associated Mouse Gene:
Fa2h
Analysis Tools