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OMIM:613454 - RETT SYNDROME, CONGENITAL VARIANT
DOID:1206 - Rett syndrome |
MONDO:0013270 - Rett syndrome, congenital variant |
Human Disease Resources: OMIM
Xenbase Genes: foxg1
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DOID:1206 - Rett syndrome |
MONDO:0013270 - Rett syndrome, congenital variant |