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