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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
SPG73 14568
spastic paraplegia 73, autosomal dominant 14568
spastic paraplegia 73, autosomal dominant; SPG73 http://purl.obolibrary.org/obo/MONDO_0014568
autosomal dominant spastic paraplegia type 73 14568
CPT1C autosomal dominant pure spastic paraplegia 14568
hereditary spastic paraplegia 73 14568
hereditary spastic paraplegia type 73 14568
autosomal dominant pure spastic paraplegia caused by mutation in CPT1C 14568
autosomal dominant spastic paraplegia 73 14568