raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:730675

Isolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin

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

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enIsolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin
frTrouble complexe du neurodéveloppement isolé sans DI/TSA d'origine génétique/génomique
deGenetisch bedingte isolierte komplexe neurologische Entwicklungsstörung ohne Intelligenzminderung oder Autismus-Spektrum-Störung
esTrastorno del neurodesarrollo complejo aislado sin discapacidad intelectual ni trastorno del espectro autista de origen genético/genómico
itMalattia complessa isolata del neurosviluppo senza ID/ADS di origine genetica/genomica
nlGeïsoleerde complexe neurologische ontwikkelingsstoornis zonder ID/ASD van genetische/genomische oorsprong
ptIsolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin
plIsolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin
csIsolated complex neurodevelopmental disorder without ID/ASD of genetic/genomic origin
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card