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Results 1 - 2 of 2 for RAD21
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  1. Cornelia de Lange syndrome 
    ... condition. Variants in other genes, including SMC1A, HDAC8, RAD21, SMC3, and others, are much less common.The ... during development.Variants in the NIPBL, SMC1A, HDAC8, RAD21, and SMC3 genes cause Cornelia de Lange syndrome ...
    https://medlineplus.gov/.../condition/cornelia-de-lange-syndrome - Genetics
  2. Trichorhinophalangeal syndrome type II 
    ... genes on chromosome 8. The TRPS1, EXT1, and RAD21 genes are missing in people with TRPS II. ... other bone and facial abnormalities. Deletion of the RAD21 gene may contribute to intellectual disability. The loss ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-ii - Genetics