MONDO_merge (183,974) Find_IDs 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

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Label
Id
achromatopsia 3; ACHM3 http://purl.obolibrary.org/obo/MONDO_0009875
achromatopsia caused by mutation in CNGB3 9875
Beckwith-Wiedemann syndrome due to 11p15 microduplication 19875
achromatopsia with myopia 9875
total colorblindness with myopia 9875
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