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    Search syndromes by name or geneSearching for: FH 
   
	
		
			| Syndrome | Synonym | Genes |  |  
			| Bone Dysplasia with Malignant Change, Hereditary | Hereditary Bone Dysplasia with Malignant Fibrous Histiocytoma, Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma, DMS-MFH | DMSMFH/BDMF# | Show details |  
			| Familial Hemophagocytic Lymphohistiocytosis | FHLH, FHL, Familial Hemophagocytic Reticulosis, FHR | HPLH1#, PRF1, RAG1, RAG2, STX11, UNC13D | Show details |  
			| Familial Hyperaldosteronism type I | Dexamethasone Sensitive Aldosteronism, FH-I | CYP11B1/2 | Show details |  
			| Familial Hyperaldosteronism type II | FH-II | FH-II# | Show details |  
			| Hereditary Leiomyomatosis and Renal Cell Cancer | HLRCC, Reed syndrome, Hereditary Multiple Leiomyomata of Skin and Uterus | FH | Show details |  
			| Renal Cell Cancer associated with constitutional translocation of chromosome 3 |  | FHIT, TRC8 | Show details |  |