Hypotonia, infantile, with psychomotor retardation and characteristic facies 1

MONDO:0024567

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

Also known as: NALCN hypotonia, infantile, with psychomotor retardation and characteristic facies, hypotonia, infantile, with psychomotor retardation and characteristic facies 1, hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in NALCN, IHPRF1, Ihprf

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 itself.

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