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ID DOID:0111841
Name Shukla-Vernon syndrome
Definition A syndrome characterized by global developmental delay, variably impaired intellectual development, variable dysmorphic features, and behavioral abnormalities, including autism spectrum disorder and ADHD that has_material_basis_in hemizygous mutation in the BCORL1 gene on chromosome Xq26.1.
https://www.ncbi.nlm.nih.gov/pubmed/30941876
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OMIM:301029

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is_a syndrome

is_a X-linked recessive disease

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