mandibulofacial dysostosis | Berry's syndrome | Franceschetti's syndrome | Franceschetti-Zwahlen syndrome | Franceschetti-Zwahlen-Klein syndrome | Zwahlen's syndrome | bilateral facial agenesis | mandibulo-facial syndrome

Franceschetti's syndrome | Franceschetti-Zwahlen syndrome

Franceschetti syndrome | Franceschetti-Zwahlen syndrome | mandibulofacial dysostosis | Treacher Collins syndrome

Franceschetti’s syndrome | mandibulofacial dysostosis | Treacher Collins syndrome

Franceschetti-Jadassohn syndrome

Korsakoff's syndrome | Korsakoff syndrome | Korsakov's syndrome | Korsakow's syndrome | alcohol amnestic disorder | alcoholic dementia | amnesic syndrome | amnestic-confabulatory syndrome | amnestic psychosis | amnestic syndrome | cerebropathia psychica toxaemica | chronic alcoholic delirium | dysmnesic psychosis | dysmnesic syndrome | Korsakoff's disease | Korsakoff's psychosis | Korsakoff psychosis | Korsakov's psychosis | Korsakow's psychosis | Korsakosis | polyneuritic insanity | polyneuritic psychosis | polyneuritic syndrome | psychosis polyneuritica

Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome

Korsakov's psychosis [ Korsakoff psychosis | Korsakoff syndrome | Korsakoff's disease | Korsakoff's syndrome | Korsakoff's amnesic syndrome | Korsakoff's amnestic syndrome ]

A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c

A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib