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Up to: Hereditary neurological disease · Neurodevelopmental disorder
Mendelian neurodevelopmental disorder
A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome.
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Genetic developmental and epileptic encephalopathy 2 trials · 83 incl. sub-types Sub-types →
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Prader-Willi syndrome 32 trials Sub-types →
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Rett syndrome 31 trials
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Intellectual disability, autosomal dominant 0 trials · 23 incl. sub-types Sub-types →
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X-linked intellectual disability 1 trial · 15 incl. sub-types Sub-types →
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CACNA1A-related complex neurodevelopmental disorder 1 trial · 9 incl. sub-types Sub-types →
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Autosomal recessive primary microcephaly 0 trials · 8 incl. sub-types Sub-types →
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Smith-Magenis syndrome 5 trials
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Rubinstein-Taybi syndrome 3 trials Sub-types →
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FOXG1 disorder 2 trials
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Orofaciodigital syndrome I 1 trial
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Dyneinopathy 0 trials · 1 incl. sub-types Sub-types →
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Intellectual disability, autosomal recessive 0 trials · 1 incl. sub-types Sub-types →
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Alzahrani-Kuwahara syndrome 0 trials
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Amish lethal microcephaly 0 trials
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Au-Kline syndrome 0 trials
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CK syndrome 0 trials
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Delpire-McNeill syndrome 0 trials
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Harel-Yoon syndrome 0 trials
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Houge-Janssens syndrome 3 0 trials
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KCNH1 associated disorder 0 trials Sub-types →
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Li-Takada-Miyake syndrome 0 trials
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Pitt-Hopkins-like syndrome 2 0 trials
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Popov-Chang syndrome 0 trials
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Stankiewicz-Isidor syndrome 0 trials
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Wieacker-Wolff syndrome 0 trials
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Squalene synthase deficiency 0 trials