ORPHA:729560
Forebrain malformation
- 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.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Forebrain malformation | |
| fr | Malformation du prosencéphale | |
| de | Vorderhirnfehlbildung | |
| es | Malformación del prosencéfalo | |
| it | Malformazione del proencefalo | |
| nl | Malformatie van voorhersenen | |
| pt | Forebrain malformation | |
| pl | Forebrain malformation | |
| cs | Forebrain malformation |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98044Central nervous system malformation
rare developmental anomalies during embryogenesis; rare neurological diseases
Children (7):
- ORPHA:269194Central nervous system cystic malformation
- ORPHA:324353Congenital achiasma
- ORPHA:48471Lissencephaly
- ORPHA:199633Non-syndromic cerebral malformation
- ORPHA:269531Other syndrome with a central nervous system malformation as a major feature
- ORPHA:199639Syndrome with corpus callosum agenesis/dysgenesis as a major feature
- ORPHA:269528Syndrome with microcephaly as a major feature
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/729560
- This record as JSON: /data/d/729560.json