Informaţii despre

Nume Calciphylaxis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificari ICD10 Disorders of calcium metabolism
Clasificare anatomică Malacards Boli cardiovasculare; Boli osoase

Vezi şi

Boli A-Z Acquired Immunodeficiency Syndrome Aging Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Angiomatosis Aniridia 1 Anorexia Nervosa 1 Arcus Corneae Arterial Calcification, Generalized, of Infancy, 1 Arterial Calcification of Infancy Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Atrial Fibrillation Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Remodeling Disease Breast Cancer Calcinosis Calciphylaxis Cutis Cerebral Atrophy Cerebritis Cholangiocarcinoma Cholesterol Embolism Chronic Myelomonocytic Leukemia Cockayne Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Connective Tissue Disease Cryofibrinogenemia Cryoglobulinemia Dermatitis Dermatomyositis Diabetes Mellitus Diffuse Dermal Angiomatosis Diffuse Lymphatic Malformation Ecthyma Endocarditis End Stage Renal Failure Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Familial Hypocalciuric Hypercalcemia Fanconi Syndrome Focal Segmental Glomerulosclerosis Galactose Epimerase Deficiency Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypervitaminosis D Hypocalcemia, Autosomal Dominant 1 Hypocalciuric Hypercalcemia, Familial, Type Ii Hypoparathyroidism Hypophosphatemia Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Impaired Renal Function Disease Intracranial Embolism Ischemia Ischemic Optic Neuropathy Kidney Disease Leukemia Livedoid Vasculopathy Liver Disease Lung Disease Lupus Erythematosus Lymphoma Mastitis Melanoma Metaphyseal Chondrodysplasia, Jansen Type Mineral Metabolism Disease Myelofibrosis Myeloma, Multiple Myopathy Nephrogenic Systemic Fibrosis Nephrolithiasis, Calcium Oxalate Nephrotic Syndrome Neuropathy Nondystrophic Myotonia Non-Secretory Myeloma Oncogenic Osteomalacia Osteitis Fibrosa Osteomalacia Osteonecrosis Osteonecrosis of the Jaw Pancreatic Cancer Pancreatitis Panniculitis Parathyroid Adenoma Parathyroid Carcinoma Parathyroid Gland Disease Pdgfrb-Associated Chronic Eosinophilic Leukemia Peritonitis Phosphorus Metabolism Disease Poems Syndrome Polyneuropathy Primary Hyperoxaluria Primary Hyperparathyroidism Protein C Deficiency Protein S Deficiency Pseudoxanthoma Elasticum Psoriatic Arthritis Pulmonary Alveolar Microlithiasis Purpura Pyoderma Pyoderma Gangrenosum Renal Osteodystrophy Rheumatoid Arthritis Rickets Secondary Hyperparathyroidism of Renal Origin Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Disease Spondyloocular Syndrome Spondylosis Systemic Lupus Erythematosus Temporal Arteritis Thrombosis Treacher Collins Syndrome 1 Uremia Urinary System Disease Vasculitis Xanthinuria, Type I