ORPHA:730415
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
This disease is described under Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic cause | |
| fr | Trouble complexe du neurodéveloppement avec dysmorphie/anomalies congénitales non-spécifique sans DI/TSA de cause génétique/génomique non encore identifiée | |
| de | Komplexe neurologische Entwicklungsstörung mit unspez. dysmorphen Merkmalen/kongenitalen Anomalien ohne IM/ASS mit bisher unbekannten ursächlichen Gendefekt | |
| es | Trastorno del neurodesarrollo complejo con rasgos dismórficos inespecíficos/anomalías congénitas sin DI/TEA de causa genética/genómica aún no identificada | |
| it | Malattia complessa del neurosviluppo con dismorfismi aspecifici/anomalie congenite senza ID/ASD di origine genetica/genomica non nota | |
| nl | Complexe NDD met aspecifieke dysmorfe kenmerken/congenitale anomalieën zonder ID/ASD met nog niet geïdentificeerde genetische/genomische oorzaak | |
| pt | Complex neurodevelopmental disorder with unspesific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic origin | |
| pl | Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic cause | |
| cs | Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of not yet identified genetic/genomic cause |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:730421Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/730415
- This record as JSON: /data/d/730415.json