ORPHA:199627
Atypical autism
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare, pervasive developmental disorder that does not fit the diagnosis for the other specific autistic spectrum disorders (autism, Asperger syndrome, Rett syndrome or childhood disintegrative disorder) and is characterized by usually milder developmental and social delay and less stereotypical autistic behavior.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Atypical autism | |
| fr | Autisme atypique | |
| de | Autismus, atypischer | |
| es | Autismo atípico | |
| it | Autismo atipico | |
| nl | Atypisch autisme | |
| pt | Autismo atípico | |
| pl | Autyzm atypowy | |
| cs | Atypický autismus | |
| uk | Атиповий аутизм | |
| zh | 非典型孤独症谱系障碍 | |
| tr | Atipik otizm |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F84.1 | E | specific | validated |
| ICD-11 | 6A02.Y | NTBT | index | validated |
| MONDO | 0016052 | E | validated | |
| UMLS | C0338986 | E | validated | |
| MedDRA | 10003747 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:168778Rare pervasive developmental disorder
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/199627
- This record as JSON: /data/d/199627.json