Rafiq syndrome

MONDO:0013624

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MAN1B1 gene.

Also known as: CDG2U, MAN1B1 autosomal recessive non-syndromic intellectual disability, RAFQS, autosomal recessive non-syndromic intellectual disability caused by mutation in MAN1B1, intellectual disability, autosomal recessive 15, mental retardation, autosomal recessive 15, mental retardation, autosomal recessive type 15, MRT15

0 clinical trials for this condition and its sub-types, 0 tagged with Rafiq syndrome itself.

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↑ Autosomal recessive non-syndromic intellectual disability (0)

Including sub-types (0) Tagged with Rafiq syndrome (0)

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