ORPHA:31709
Infantile convulsions and choreoathetosis
inactive · moved to ORPHA:306Self-limited infantile epilepsy
Synonyms: ICCA syndrome · Paroxysmal kinesigenic dyskinesia and infantile convulsions
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Self-limited infantile epilepsy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infantile convulsions and choreoathetosis | ICCA syndrome · Paroxysmal kinesigenic dyskinesia and infantile convulsions |
| fr | Syndrome de convulsions infantiles-choréoathétose | Syndrome ICCA |
| de | Infantile Konvulsionen und Choreoathetose | ICCA-Syndrom · Paroxysmale kinesiogene Dyskinesie mit infantilen Konvulsionen |
| es | Crisis del lactante con coreoatetosis | Discinesia paroxística cinesigénica y crisis del lactante · Síndrome ICCA |
| it | Convulsioni infantili e coreoatetosi | Discinesia chinesigenica parossistica e convulsioni infantili · Sindrome ICCA |
| nl | Infantiele convulsies en choreoathetose | ICCA-syndroom · Paroxysmale kinesigene dyskinesie en infantiele convulsies |
| pt | Convulsões e coreoatetose do lactente | Síndrome ICCA |
| pl | Zespół drgawek dziecięcych i choreoatetozy | Napadowa kinezygenna dyskineza i drgawki dziecięce · Zespół ICCA |
| cs | Infantilní konvulze a choreoatetóza | ICCA syndrom · Paroxysmální kinezigenní dyskineze a infantilní konvulze |
| uk | Інфантильні судоми з хореоатетозом | Синдром ICCA · Пароксизмальна кінезигенна дискінезія та дитячі судоми |
| zh | 婴儿惊厥和舞蹈手足徐动症 | 发作性运动诱发性运动障碍和婴儿惊厥症 |
| tr | İnfantil konvülsiyonlar ve koreoatetoz | ICCA sendromu · Paroksismal kinesigenik diskinezi ve infantil konvülsiyonlar |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0011178 | E | validated | |
| MeSH | C535522 | E | validated | |
| UMLS | C1865926 | E | validated | |
| GARD | 8553 | 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
Not placed in any Orphanet classification in this release.
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/31709
- This record as JSON: /data/d/31709.json