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
limb-girdle, type 2g muscular dystrophy C566599
pyogenic iliopsoas abscesses D016659
myopia, and sensorineural deafness spondyloepiphyseal dysplasia C566659
thrombocytosis, benign familial microcytic C566596
abscess, pyogenic iliopsoas D016659
abscesses, pyogenic iliopsoas D016659
muscular dystrophy, limb-girdle, type 2g C566599
benign familial microcytic thrombocytosis C566596
ectodermal dysplasia, pure hair-nail type C566592
iliopsoas abscess, pyogenic D016659
iliopsoas abscesses, pyogenic D016659
intestinal, with secondary hypocalcemia hypomagnesemia C566593
8p23.1 duplication syndrome 16659
pure hair-nail type ectodermal dysplasia C566592