{"orpha":730415,"name":"Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies 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 Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder","url":"https://raremap.alftech.space/d/ORPHA-730415/","orphanet_url":"https://www.orpha.net/en/disease/detail/730415","names":{"fr":{"name":"Trouble complexe du neurodéveloppement avec dysmorphie/anomalies congénitales non-spécifique sans DI/TSA de cause génétique/génomique non encore identifiée"},"de":{"name":"Komplexe neurologische Entwicklungsstörung mit unspez. dysmorphen Merkmalen/kongenitalen Anomalien ohne IM/ASS mit bisher unbekannten ursächlichen Gendefekt"},"es":{"name":"Trastorno del neurodesarrollo complejo con rasgos dismórficos inespecíficos/anomalías congénitas sin DI/TEA de causa genética/genómica aún no identificada"},"it":{"name":"Malattia complessa del neurosviluppo con dismorfismi aspecifici/anomalie congenite senza ID/ASD di origine genetica/genomica non nota"},"nl":{"name":"Complexe NDD met aspecifieke dysmorfe kenmerken/congenitale anomalieën zonder ID/ASD met nog niet geïdentificeerde genetische/genomische oorzaak"},"pt":{"name":"Complex neurodevelopmental disorder with unspesific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic origin"},"pl":{"name":"Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic cause"},"cs":{"name":"Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic cause"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":730421,"name":"Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder","classifications":[147,156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}