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
Label
Id
ACHM2 9003
MEN2 19003
RMCH2 9003
CNGA3 achromatopsia 9003
achromatopsia 2 9003
colorblindness, total 9003
Rod monochromacy 2 9003
Rod monochromatism 2 9003
achromatopsia type 2 9003
rod monochromacy 2 9003
rod monochromatism 2 9003
achromatopsia 2; ACHM2 http://purl.obolibrary.org/obo/MONDO_0009003
achromatopsia caused by mutation in CNGA3 9003
multiple endocrine neoplasia type 2 19003