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
mental retardation, X-linked, syndromic type 10 C3266731
HSD10 mitochondrial disease, X-linked dominant C3266731
chorioathetosis with mental retardation and abnormal behavior C3266731
chorioathetosis with mental retardation and abnormal behaviour C3266731
mental retardation with chorioathetosis and abnormal behavior C3266731
mental retardation with chorioathetosis and abnormal behaviour C3266731