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
autoimmune polyendocrinopathy type 2 10012
NAA10 X-linked syndromic intellectual disability 100124
"congenital myopathy with """"corona"""" fibers, selective muscle atrophy, and craniosynostosis" 100121
congenital myopathy with severe fetal hypokinesia 100121
PGA 2 10012