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MIM:612319 - SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE, WITH OR WITHOUT NEURODEGENERATION; SPG35
Xenbase Genes: fa2h
Human Disease Resource: MIM
MONDO:0012866 - hereditary spastic paraplegia 35 |
DOID:0110786 - hereditary spastic paraplegia 35 |
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MONDO:0012866 - hereditary spastic paraplegia 35 |
DOID:0110786 - hereditary spastic paraplegia 35 |