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Search syndromes by name or gene
Searching for: CA2
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Fanconi Anemia FILE UNDER CONSTRUCTION
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Pancytopenia Dysmelia, FA (several complementation groups)
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BRCA2, FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG/XRCC9, FANCI, FANCJ, FANCL, FANCM, FANCP/SLX4, PALB2/FANCN
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Fanconi Anemia type D1, bi-allelic BRCA2 mutations
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FANCD1
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BRCA2
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Hereditary Breast-Ovarian Cancer, BRCA2 type
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BRCA2
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Hereditary Prostate Cancer
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HPC
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BRCA2, CAPB/PCBC/EPHB2, EHBP1/HPC12, ELAC2/HPC2, HNF1B/HPC11, HOXB13, HPC1/HPT1/PRCA1/RNASEL, HPC10, HPC14, HPC15, HPC3, HPC4, HPC5, HPC6, HPC7, HPC9, HPCX1, HPCX2, MSMB/HPC13, PCA3/DD3, PCAP/HPC8
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Li-Fraumeni syndrome
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LFS, SBLA syndrome (Sarcoma Breast Leukemia Adrenal cancer), incl.: Cancer with In Vitro Radioresistence, Familial, Li-Fraumeni-like s.
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BRCA2, TP53
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Oculocutaneous Albinism
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OCA1, OCA2, TYRP1
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Pancreatic Cancer, Familial Clustering of
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incl.: Hereditary Pancreatic Adenocarcinoma, Insulin-Dependent Diabetes Mellitus - Exocrine Insufficiency - Familial Pancreatic Cancer, PNCA1
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ATM, BRCA2, PALB2/FANCN, PALLD
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