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

There is 0 pattern entry.

Label
Id
LGMD2O 13161
MDDGC3 13161
LGMD-POMGNT1 related 13161
rupture, splenic D013161
ruptures, splenic D013161
splenic rupture D013161
splenic ruptures D013161
POMGNT1 autosomal recessive limb-girdle muscular dystrophy 13161
limb-girdle muscular dystrophy type 2O 13161
muscular dystrophy-dystroglycanopathy (limb-girdle) type C3 13161
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3 13161
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3; MDDGC3 http://purl.obolibrary.org/obo/MONDO_0013161
muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related 13161
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1 13161
autosomal recessive limb-girdle muscular dystrophy type 2O 13161
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