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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
autosomal recessive limb-girdle muscular dystrophy caused by mutation in LIMS2 14788
autosomal recessive limb-girdle muscular dystrophy type 2W 14788
autosomal recessive limb-girdle muscular dystrophy type 2X 14782
autosomal recessive limb-girdle muscular dystrophy-cardiac arrhythmia syndrome 14782
muscular dystrophy, limb-girdle, type 2W 14788
muscular dystrophy, limb-girdle, type 2W; LGMD2W http://purl.obolibrary.org/obo/MONDO_0014788
muscular dystrophy, limb-girdle, type 2X 14782
muscular dystrophy, limb-girdle, type 2X; LGMD2X http://purl.obolibrary.org/obo/MONDO_0014782
muscular dystrophy, limb-girdle, type 2w 14788
muscular dystrophy, limb-girdle, type 2x 14782
nasopharynx benign neoplasm 21478
benign neoplasm of nasopharynx 21478
benign tumor of nasopharynx 21478
benign neoplasm of the nasopharynx 21478
congenital disorder of glycosylation type 2o 14789