Hypotonia, infantile, with psychomotor retardation and characteristic facies 2

Any hypotonia, infantile, with psychomotor retardation and characteristic facies in which the cause of the disease is a mutation in the UNC80 gene.

Also known as: IHPRF2, UNC80 hypotonia, infantile, with psychomotor retardation and characteristic facies, hypotonia, infantile, with psychomotor retardation and characteristic facies 2, hypotonia, infantile, with psychomotor retardation and characteristic facies 2; IHPRF2, hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in UNC80, hypotonia, infantile, with psychomotor retardation and characteristic facies type 2

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotonia, infantile, with psychomotor retardation and characteristic facies 2 itself.