{"orpha":93943,"name":"Corpus callosum dysgenesis-hypopituitarism syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Septo-optic dysplasia spectrum","url":"https://raremap.alftech.space/d/ORPHA-93943/","orphanet_url":"https://www.orpha.net/en/disease/detail/93943","names":{"fr":{"name":"Syndrome de dysgénésie du corps calleux-hypopituitarisme"},"de":{"name":"Corpus-callosum-Dysgenesie mit Hypopituitarismus"},"es":{"name":"Síndrome de disgenesia del cuerpo calloso-hipopituitarismo"},"it":{"name":"Disgenesia del corpo calloso - ipopituitarismo"},"nl":{"name":"Dysgenesie van corpus callosum - hypopituïtarisme-syndroom"},"pt":{"name":"Síndrome de disgenesia do corpo caloso-hipopituitarismo"},"pl":{"name":"Dysgenezja ciała modzelowatego - niedoczynność przysadki"},"cs":{"name":"Syndrom zahrnující dysgenezi corpus callosum a hypopituitarismus"},"uk":{"name":"Синдром дисгенезії мозолистого тіла - гіпопітуїтаризм"},"zh":{"name":"胼胝体发育不全-垂体功能减退症"},"tr":{"name":"Korpus kallozum disgenezi-hipopituitarizm sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":3157,"name":"Septo-optic dysplasia spectrum"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}