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

There is 0 pattern entry.

Label
Id
achromatopsia type 2 C1857618
rod monochromacy 2 C1857618
rod monochromatism 2 C1857618
Total color blindness C1857618
achromatopsia caused by mutation in CNGA3 C1857618
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