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HIDEA syndrome is a syndrome characterised by hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities. It is caused by the mutation of the P4HTM gene on chromosome 3.

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  • HIDEA syndrome is a syndrome characterised by hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities. It is caused by the mutation of the P4HTM gene on chromosome 3. (en)
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  • HIDEA syndrome is inherited via an autosomal recessive manner. (en)
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  • Mutation in P4HTM gene (en)
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  • HIDEA syndrome (en)
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  • HIDEA syndrome is a syndrome characterised by hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities. It is caused by the mutation of the P4HTM gene on chromosome 3. (en)
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  • HIDEA syndrome (en)
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  • HIDEA syndrome (en)
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