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Brachydactyly type A4, Brachydactyly type A5, Brachydactyly type A6, Brachydactyly type A7, Brachydactyly

type B, Brachydactyly type C, Brachydactyly type E, Brachydactyly types B and E combined, Brachydactyly

with hypertension, Brachymesomelia renal syndrome, Brachymesophalangy type 2, Brachymetapody

anodontia hypotrichosis albinoidism, Brachyolmia type 1 Hobaek type, Brachyolmia type 3, Brachyphalangy

polydactyly and tibial aplasia/hypoplasia, Braddock Jones Superneau syndrome, Brain stem cancer, Brain

stem glioma childhood, Brain tumor adult, Brain tumor childhood, Branchial arch defects, Branchial arch

syndrome X-linked, Branchiooculofacial syndrome, Branchiootic syndrome, Branchiootorenal syndrome,

Breast cancer childhood, Breast cancer male, Brenner tumor of ovary, Brenner tumor of the vagina, Brittle

bone syndrome lethal type, Brittle cornea syndrome, Broad-betalipoproteinemia, Brody myopathy, Bronchial

adenomas/carcinoids childhood, Bronchiectasis oligospermia, Bronchiolitis obliterans, Bronchiolitis obliterans

organizing pneumonia, Bronchogenic cyst, Bronchopulmonary dysplasia, Brooks Wisniewski Brown

syndrome, Brown syndrome, Brown-Sequard syndrome, Brown-Vialetto-Van laere syndrome, Brucellosis,

Bruck syndrome 1, Bruck syndrome 2, Brugada syndrome, Brugada syndrome 3, Brugada syndrome 4,

Brunoni syndrome, Brunsting-Perry syndrome, Bruyn Scheltens syndrome, Bubonic plague, Budd-Chiari

syndrome, Buerger disease, Bulbo-spinal atrophy X-linked, Bulbospinal amyotrophy X-linked, Bullous

dystrophy hereditary macular type, Bullous erythroderma ichthyosiformis congenita of Brocq, Bullous

pemphigoid, Burkitt's lymphoma, Burn Goodship syndrome, Burn-Mckeown syndrome, Burnett Schwartz

Berberian syndrome, Burning mouth syndrome type 3, Buruli ulcer, Buschke Lowenstein tumor, Buschke

Ollendorff syndrome, Bustos Simosa Pinto Cisternas syndrome, Butyrylcholinesterase deficiency, Byssinosis,

C syndrome

Rare Diseases and Disorders - Starting With "C"

C-like syndrome, CADASIL, Cafe au lait spots multiple, Caffey disease, CAHMR syndrome, Calabro

syndrome, Calcifying Epithelial Odontogenic Tumor, Calciphylaxis, California encephalitis, Calloso-genital

dysplasia, Calvarial hyperostosis, Camera Marugo Cohen syndrome, Campomelia Cumming type,

Campomelic dysplasia, Camptobrachydactyly, Camptocormism, Camptodactyly arthropathy coxa vara

pericarditis syndrome, Camptodactyly joint contractures and facial skeletal dysplasia, Camptodactyly

syndrome Guadalajara type 1, Camptodactyly syndrome Guadalajara type 2, Camptodactyly syndrome

Guadalajara type 3, Camptodactyly taurinuria, Camptodactyly vertebral fusion, Camptodactyly fibrous tissue

hyperplasia and skeletal dysplasia, Camptodactyly tall stature and hearing loss syndrome,

Camptodactyly-ichthyosis syndrome, Camptomelic syndrome long limb type, Camurati Engelmann disease

type 2, Camurati-Engelmann disease, Canavan disease, Candida glabrata, Candidiasis familial chronic

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