ORPHA:730679
Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Isolated complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause | |
| fr | Trouble complexe du neurodéveloppement isolé sans DI/TSA de cause génétique/génomique non encore identifiée | |
| de | Isolierte komplexe neurologische Entwicklungsstörung ohne Intelligenzminderung oder Autismus-Spektrum-Störung mit bisher unbekannten ursächlichen Gendefekt | |
| es | Trastorno del neurodesarrollo complejo aislado sin discapacidad intelectual ni trastorno del espectro autista de causa genética/genómica aún no identificada | |
| it | Malattia complessa isolata del neurosviluppo senza ID/ADS di origine genetica/genomica non nota | |
| nl | Geïsoleerde complexe neurologische ontwikkelingsstoornis zonder ID/ASD met nog niet geïdentificeerde genetische/genomische oorzaak | |
| pt | Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic origin | |
| pl | Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause | |
| cs | Isolated complex neurodevelopmental disorder without ID/ASD of not yet identified genetic/genomic cause |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:730672Isolated complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder
rare genetic diseases; rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/730679
- This record as JSON: /data/d/730679.json