ORPHA:102010
Other syndrome with lissencephaly as a major feature
- 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 | Other syndrome with lissencephaly as a major feature | |
| fr | Autre syndrome avec une lissencéphalie comme manifestation majeure | |
| de | Sonstige Syndrome mit Lissenzephalie als Hauptmerkmal | |
| es | Otros síndromes con lisencefalia como característica principal | |
| it | Altra sindrome con lissencefalia come segno cardinale | |
| nl | Ander syndroom met lissencefalie als hoofdkenmerk | |
| pt | Outro síndrome com lisencefalia como característica principal | |
| pl | Inny zespół z lizencefalią jako głównym objawem | |
| cs | Další syndromy s lisencefalií jako hlavním příznakem | |
| uk | Інші синдроми з лісенцефалією як основною ознакою | |
| zh | 其他以无脑回畸形为主要特征的综合征 | |
| tr | Esas klinik özelliği lizensefali olan diğer sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD20.1 | E | specific | validated |
| MONDO | 15147 | E | validated | |
| UMLS | C5681781 | E | validated | |
| GARD | 19820 | 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 (1):
- ORPHA:48471Lissencephaly
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:101356OBSOLETE: Lissencephaly-demyelinating axonal neuropathy syndrome referred to · inactive
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/102010
- This record as JSON: /data/d/102010.json