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

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Label
Id
amish nemaline myopathy C538397
nemaline myopathy, amish type C538397
amish type nemaline myopathy C538397
caused by mutation in the troponin t1 gene nemaline myopathy C538397
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