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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
LGMD2I 11787
MDDGC5 11787
LGMD-FKRP related 11787
muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related 11787
muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 5 11787
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5 11787
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5 11787
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5; MDDGC5 http://purl.obolibrary.org/obo/MONDO_0011787
limb-girdle muscular dystrophy due to FKRP deficiency 11787
limb-girdle muscular dystrophy type 2I 11787
autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKRP 11787
autosomal recessive limb-girdle muscular dystrophy type 2I 11787
muscular dystrophy limb-girdle type 2I 11787
muscular dystrophy-dystroglycanopathy, limb-girdle, Frkp-Related http://purl.obolibrary.org/obo/MONDO_0011787
muscular dystrophy-dystroglycanopathy, limb-girdle, Frkp-related 11787