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
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
hyperphosphatasia with mental retardation syndrome 6 14780
hyperphosphatasia with mental retardation syndrome type 6 14780
benign nasopharyngeal neoplasm 21478
nasopharynx benign neoplasm 21478
congenital disorder of glycosylation type 2o 14789
congenital disorder of glycosylation type IIo 14789
congenital disorder of glycosylation, type IIo 14789
benign neoplasm of nasopharynx 21478