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ENSmith-Mccort Dysplasia 2 (SMC2)
Alias:
Smc2
Dysplasia, Smith-Mccort, Type 2
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Smith-Mccort Dysplasia 2, also known as smc2, is related to cornelia de lange syndrome and fanconi anemia, complementation group i. An important gene associated with Smith-Mccort Dysplasia 2 is RAB33B (RAB33B, Member RAS Oncogene Family). Affiliated tissues include bone and smooth muscle, and related phenotypes are short neck and hyperlordosis
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MALACARDS
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