MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
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
SPG8 11339
autosomal dominant spastic paraplegia type 8 11339
spastic paraplegia 8 11339
spastic paraplegia 8, autosomal dominant 11339
spastic paraplegia 8, autosomal dominant; SPG8 http://purl.obolibrary.org/obo/MONDO_0011339
hereditary spastic paraplegia 8 11339
hereditary spastic paraplegia caused by mutation in WASHC5 11339
hereditary spastic paraplegia type 8 11339
WASHC5 hereditary spastic paraplegia 11339
autosomal dominant spastic paraplegia 8 11339