{"orpha":730679,"name":"Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This disease is described under Isolated complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder","url":"https://raremap.alftech.space/d/ORPHA-730679/","orphanet_url":"https://www.orpha.net/en/disease/detail/730679","names":{"fr":{"name":"Trouble complexe du neurodéveloppement isolé sans DI/TSA de cause génétique/génomique non encore identifiée"},"de":{"name":"Isolierte komplexe neurologische Entwicklungsstörung ohne Intelligenzminderung oder Autismus-Spektrum-Störung mit bisher unbekannten ursächlichen Gendefekt"},"es":{"name":"Trastorno del neurodesarrollo complejo aislado sin discapacidad intelectual ni trastorno del espectro autista de causa genética/genómica aún no identificada"},"it":{"name":"Malattia complessa isolata del neurosviluppo senza ID/ADS di origine genetica/genomica non nota"},"nl":{"name":"Geïsoleerde complexe neurologische ontwikkelingsstoornis zonder ID/ASD met nog niet geïdentificeerde genetische/genomische oorzaak"},"pt":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic origin"},"pl":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause"},"cs":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":730672,"name":"Isolated complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder","classifications":[156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}