MONDO_merge Find_IDs Find_Terms Annotation
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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
FSP3 10878
SPG6 10878
hereditary spastic paraplegia 6 10878
spastic paraplegia 6, autosomal dominant 10878
spastic paraplegia 6, autosomal dominant; SPG6 http://purl.obolibrary.org/obo/MONDO_0010878
autosomal dominant familial spastic paraplegia type 3 10878
spastic paraplegia 6 10878
familial spastic paraplegia autosomal dominant 3 10878
hereditary spastic paraplegia caused by mutation in NIPA1 10878
hereditary spastic paraplegia type 6 10878
familial spastic paraplegia, autosomal dominant, 3 10878
autosomal dominant spastic paraplegia type 6 10878
NIPA1 hereditary spastic paraplegia 10878
autosomal dominant spastic paraplegia 6 10878