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mental retardation, nonsyndromic autosomal dominant 2 (MRD2)
Genetics: - autosomal dominant form associated with defects in DOCK8 Clinical manifestations: - non-specific (see mental retardation) - sub-average general intellectual functioning associated with impairments in adaptative behavior - manifested during the developmental periodDatabase Correlations
OMIM 614113]References
- OMIM :accession 614113]