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MIM:616803 - LAMB-SHAFFER SYNDROME; LAMSHF
Xenbase Genes: sox5
Human Disease Resource: OMIM
MONDO:0014778 - Lamb-Shaffer syndrome |
MONDO:0017781 - 12p12.1 microdeletion syndrome |
MONDO:0017782 - developmental and speech delay due to SOX5 deficiency |