{"orpha":730707,"name":"Genetic forebrain malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-730707/","orphanet_url":"https://www.orpha.net/en/disease/detail/730707","names":{"fr":{"name":"Malformation du prosencéphale génétique"},"de":{"name":"Fehlbildung des Prosencephalon, genetische bedingte"},"es":{"name":"Malformación genética del prosencéfalo"},"it":{"name":"Malformazione genetica del proencefalo"},"nl":{"name":"Genetische malformatie van voorhersenen"},"pt":{"name":"Genetic forebrain malformation"},"pl":{"name":"Genetic forebrain malformation"},"cs":{"name":"Genetic forebrain malformation"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183506,"name":"Genetic central nervous system malformation","classifications":[156]}],"children":[{"orpha":530033,"name":"Dermoid or epidermoid cyst of the central nervous system","type":"Morphological anomaly"},{"orpha":269553,"name":"Genetic cerebral malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}