All individuals with variants in gene TBC1D20

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00261173 Fam7 Journal: Fischer-Zirnsak 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - DD developmental delay/intellectual disability (HP:0012758/HP:0001249); autism spectrum disorder (HP:0000729); attention deficit hyperactivity disorder (HP:0007018); no stereotypic behavior (-HP:0000733); no seizures (-HP:0001250); muscular hypotonia (HP:0001252); no ataxia (-HP:0001251); no abnormal prenatal brain imaging; microcephaly (HP:0000252); no macrocephaly (-HP:0000256); facial dysmorphism (HP:0000271);  small joint hypermobility 1 1 Johan den Dunnen
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