ORPHA:730418

Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of genetic/genomic origin

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

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 genetic/genomic origin
fr	Trouble complexe du neurodéveloppement avec dysmorphie/anomalies congénitales non-spécifique sans DI/TSA d'origine génétique/génomique
de	Genetisch bedingte komplexe neurologische Entwicklungsstörung mit unspez. dysmorphen Merkmalen/kongenitalen Anomalien ohne IM/ASS
es	Trastorno del neurodesarrollo complejo con rasgos dismórficos inespecíficos/anomalías congénitas sin discapacidad intelectual/TEA de origen genético/genómico
it	Malattia complessa del neurosviluppo con dismorfismi aspecifici/anomalie congenite senza ID/ASD di origine genetica/genomica
nl	Complexe neurologische ontwikkelingsstoornis met aspecifieke dysmorfe kenmerken/congenitale anomalieën zonder ID/ASD van genetische/genomische oorsprong
pt	Complex neurodevelopmental disorder with unspesific dysmorphic features/congenital anomalies without ID/ASD of genetic/genomic origin
pl	Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of genetic/genomic origin
cs	Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without ID/ASD of genetic/genomic origin

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

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.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/730418
This record as JSON: /data/d/730418.json