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Monogenic disease
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facioscapulohumeral muscular dystrophy | |
Faisalabad histiocytosis | |
familial atypical mycobacteriosis | |
familial capillary malformation-arteriovenous (...) | |
familial esophageal achalasia | |
familial glomuvenous malformation | |
familial hemophagocytic lymphohistiocytosis | |
familial mediterranean fever | |
familial megacalyces | |
familial schwannomatosis | |
familial spina bifida | |
familial splenic asplenia/hypoplasia | |
familial thrombotic thrombocytopenic purpura | |
Fanconi disease | |
Feingold syndrome | |
FENIB | |
fibrodysplasia ossificans progressiva | |
FKTN | |
Francois-Neetens fleck corneal dystrophy | |
Frasier syndrome | |
Friedreich ataxia | |
FTDP-17 | |
fucosidosis |