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
Alpha-sarcoglycanopathy 11968
DMDA2 11968
LGMD2D 11968
Adhalinopathy, primary 11968
primary adhalinopathy 11968
SGCA autosomal recessive limb-girdle muscular dystrophy 11968
limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency 11968
limb-girdle muscular dystrophy type 2D 11968
limb-girdle muscular dystrophy, type 2D 11968
autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA 11968
autosomal recessive limb-girdle muscular dystrophy type 2D 11968
muscular dystrophy, limb-girdle, type 2D 11968
muscular dystrophy limb-girdle with alpha-sarcoglycan 11968
muscular dystrophy, limb-girdle, type 2D; LGMD2D http://purl.obolibrary.org/obo/MONDO_0011968
Duchenne-like autosomal recessive muscular dystrophy type 2 11968