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
LGMD2N 13162
MDDGC2 13162
LGMD-POMT2 related 13162
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2 13162
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2 13162
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2; MDDGC2 http://purl.obolibrary.org/obo/MONDO_0013162
limb-girdle muscular dystrophy type 2N 13162
muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related 13162
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2 13162
autosomal recessive limb-girdle muscular dystrophy type 2N 13162
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-Related http://purl.obolibrary.org/obo/MONDO_0013162
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related 13162
muscular dystrophy, limb-girdle, type 2N 13162
POMT2 autosomal recessive limb-girdle muscular dystrophy 13162