Mondo_2019_Kim Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries
Label
Id
Alpha-sarcoglycanopathy http://purl.obolibrary.org/obo/MONDO_0011968
DMDA2 http://purl.obolibrary.org/obo/MONDO_0011968
LGMD2D http://purl.obolibrary.org/obo/MONDO_0011968
Adhalinopathy, primary http://purl.obolibrary.org/obo/MONDO_0011968
primary adhalinopathy http://purl.obolibrary.org/obo/MONDO_0011968
limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency http://purl.obolibrary.org/obo/MONDO_0011968
limb-girdle muscular dystrophy type 2D http://purl.obolibrary.org/obo/MONDO_0011968
limb-girdle muscular dystrophy, type 2D http://purl.obolibrary.org/obo/MONDO_0011968
autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA http://purl.obolibrary.org/obo/MONDO_0011968
autosomal recessive limb-girdle muscular dystrophy type 2D http://purl.obolibrary.org/obo/MONDO_0011968
muscular dystrophy limb-girdle with alpha-sarcoglycan http://purl.obolibrary.org/obo/MONDO_0011968
muscular dystrophy, limb-girdle, type 2D http://purl.obolibrary.org/obo/MONDO_0011968
muscular dystrophy, limb-girdle, type 2D; LGMD2D http://purl.obolibrary.org/obo/MONDO_0011968
SGCA autosomal recessive limb-girdle muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0011968
Duchenne-like autosomal recessive muscular dystrophy type 2 http://purl.obolibrary.org/obo/MONDO_0011968