MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries
Label
Id
ACHM1 C1849792
ACHM3 C1849792
Achm3 C1849792
Pingelapese C1849792
RMCH1 C1849792
Achromatopsia with myopia C1849792
Rod monochromacy 1 (formerly) C1849792
Rod monochromatism 1 (formerly) C1849792
ROD MONOCHROMACY 1, FORMERLY C1849792
ROD MONOCHROMATISM 1, FORMERLY C1849792
rod monochromacy 1, formerly C1849792
rod monochromatism 1, formerly C1849792
achromatopsia caused by mutation in CNGB3 C1849792
ROD MONOCHROMACY 1 C1849792
ROD MONOCHROMATISM 1 C1849792