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Start free with EleplanComplex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder
ORPHA:730421Disease
What it is
A rare neurodevelopmental disorder characterized by the combination of at least two neurodevelopmental disorders, including specific learning disorder (e.g., impairment in reading, written expression, or mathematics), motor disorder (e.g. developmental coordination disorder, stereotypic movement disorder, tic disorder), communication disorder (e.g., developmental language disorder, speech sound disorder, childhood-onset fluency disorder, social/pragmatic communication disorder), attention deficit/hyperactivity disorder (ADD/ADHD) and other specified or unspecified neurodevelopmental disorders as defined in DSM-5 or ICD-11. Patients don't reach the criteria of an autism spectrum disorder diagnosis, do not have intellectual disability but can present with unspecific dysmorphic features and/or congenital anomalies.
Key facts
- Classified as
- Disease
Recorded for the broader condition
- Prevalence
- 1-9 / 100 000 (France)Rare developmental defect during embryogenesis
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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