{"orpha":730675,"name":"Isolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin","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-730675/","orphanet_url":"https://www.orpha.net/en/disease/detail/730675","names":{"fr":{"name":"Trouble complexe du neurodéveloppement isolé sans DI/TSA d'origine génétique/génomique"},"de":{"name":"Genetisch bedingte isolierte komplexe neurologische Entwicklungsstörung ohne Intelligenzminderung oder Autismus-Spektrum-Störung"},"es":{"name":"Trastorno del neurodesarrollo complejo aislado sin discapacidad intelectual ni trastorno del espectro autista de origen genético/genómico"},"it":{"name":"Malattia complessa isolata del neurosviluppo senza ID/ADS di origine genetica/genomica"},"nl":{"name":"Geïsoleerde complexe neurologische ontwikkelingsstoornis zonder ID/ASD van genetische/genomische oorsprong"},"pt":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin"},"pl":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin"},"cs":{"name":"Isolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin"}},"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}