Any intellectual disability in which the cause of the disease is a mutation in the PPP2R1A gene.
Comprehensive, easy-to-understand information about this condition
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microcephaly and chorioretinopathy
MONDO:0000181
syndromic intellectual disability
MONDO:0000508
non-syndromic intellectual disability
MONDO:0000509
microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
MONDO:0007918
autosomal dominant primary microcephaly
MONDO:0007988
Prader-Willi syndrome
MONDO:0008300