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Syndromic X-linked intellectual disability Chudley-Schwartz type
MONDO:0010462A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has material basis in variation in the chromosomal region Xq21.33-q23.
Also known as: MRXSCS, X-linked intellectual disability with seizures, hypogammaglobinemia, and gait disturbance, intellectual disability, X-linked, syndromic, Chudley-Schwartz type, mental retardation, X-linked, syndromic, Chudley-Schwartz type, mental retardation, X-linked, syndromic, Chudley-Schwartz type, X-linked recessive, intellectual disability, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance, mental retardation, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance
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