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
corneal dystrophy, lattice type II C000657784
familial amyloid polyneuropathy type iv C000657784
retinitis pigmentosa, juvenile, aipl1-related C565778
juvenile, aipl1-related retinitis pigmentosa C565778
syndrome associated with hypothyroidism 15778