ORPHA:168778
Rare pervasive developmental disorder
Synonyms: Rare ASD · Rare PDD · Rare autism spectrum disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare pervasive developmental disorder | Rare ASD · Rare PDD · Rare autism spectrum disorder |
| fr | Trouble envahissant du développement rare | TED rare · Trouble rare du spectre de l'autisme |
| de | Seltene tiefgreifende Entwicklungsstörung | Seltene Autismusspektrumstörung |
| es | Trastorno generalizado raro del desarrollo | TEA raro · TGD raro · Trastorno raro del espectro autista |
| it | Disturbo pervasivo dello sviluppo raro | Disturbi rari dello spettro dell'autismo |
| nl | Zeldzame pervasieve ontwikkelingsstoornis | Zeldzame ASS · Zeldzame POS · Zeldzame autismespectrumstoornis |
| pt | Doença global do desenvolvimento | |
| pl | Rzadkie złożone zaburzenia rozwoju | Rzadkie zaburzenie spektrum autyzmu |
| cs | Vzácné pervazivní vývojové poruchy | Vzácné ASD · Vzácné PDD · Vzácná porucha autistického spektra |
| uk | Рідкісний первазивний розлад розвитку | Рідкісний аутизм · Рідкісний розлад аутистичного спектру · Рідкісні PDD |
| zh | 罕见全面发育障碍 | 罕见自闭症谱系障碍 |
| tr | Nadir yaygın gelişimsel bozukluk | Nadir ASD · Nadir PDD · Nadir otizm spektrum bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15680 | E | validated | |
| MeSH | D002659 | E | validated | |
| UMLS | C5679581 | E | validated | |
| MedDRA | 10061345 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:71859Rare genetic neurological disorder
rare genetic diseases - ORPHA:98033Rare neurologic disease with psychiatric involvement
rare neurological diseases
Children (8):
- ORPHA:3095Atypical Rett syndrome
- ORPHA:199627Atypical autism
- ORPHA:505652CDKL5-deficiency disorder
- ORPHA:168782Childhood disintegrative disorder
- ORPHA:561854FOXG1 syndrome
- ORPHA:600663NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance
- ORPHA:180772Rare disease with autism
- ORPHA:778Rett syndrome
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/168778
- This record as JSON: /data/d/168778.json