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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
combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay C567641
roifman-chitayat syndrome C567641
facial dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay combined immunodeficiency C567641