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Nume Bone Mineral Density Quantitative Trait Locus 8
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Boli A-Z Ablepharon-Macrostomia Syndrome Acquired Immunodeficiency Syndrome Acromegaly Acth-Secreting Pituitary Adenoma Adenoma Adenosine Deaminase Deficiency Adrenal Adenoma Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Aging Alcohol Abuse Allergic Rhinitis Alopecia Alopecia Areata Alopecia, Congenital Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Aminoaciduria Anauxetic Dysplasia 1 Angioedema Aniridia 1 Ankylosis Anorexia Nervosa 1 Anterior Uveitis Arterial Calcification, Generalized, of Infancy, 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrophic Gastritis Atrophic Rhinitis Autoimmune Disease Autoimmune Hepatitis Autoimmune Hypoparathyroidism Autonomic Dysfunction Back Pain Beta-Thalassemia Bladder Cancer 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 Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 16 Bone Mineral Density Quantitative Trait Locus 18 Brachydactyly Breast Cancer Brittle Bone Disorder Bronchiectasis Calcinosis Capillary Malformations, Congenital Carney Complex Variant Cataract Celiac Disease 1 Cerebritis Cerebrotendinous Xanthomatosis Cervicitis Chiari Malformation Cholangitis Cholesteatoma Chudley-Mccullough Syndrome Cohen-Gibson Syndrome Colitis Complex Regional Pain Syndrome Connective Tissue Disease Cutis Laxa Cystic Fibrosis Cytomegalovirus Infection Dementia Dentinogenesis Imperfecta Dermatomyositis Diabetes Mellitus Differentiated Thyroid Carcinoma Diffuse Idiopathic Skeletal Hyperostosis Diffuse Lymphatic Malformation Donnai-Barrow Syndrome Down Syndrome Eating Disorder Eclampsia Ehlers-Danlos Syndrome Empty Sella Syndrome Endometrial Cancer Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epilepsy Epithelial Recurrent Erosion Dystrophy Epithelioid Sarcoma Exostosis Exudative Vitreoretinopathy Familial Mediterranean Fever Fascioliasis Fecal Incontinence Fibrous Dysplasia Gastritis Genitopatellar Syndrome Germ Cells Tumors Gingivitis Glaucoma-Related Pigment Dispersion Syndrome Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glossodynia Glucocorticoid-Induced Osteoporosis Gout Graves' Disease Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy Growth Hormone Deficiency Gynecomastia Hajdu-Cheney Syndrome Hansen's Disease Hemangioma Hemiplegia Hemophilic Arthropathy Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Histiocytosis Homocystinuria Hyperostosis Hyperostosis Frontalis Interna Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypervitaminosis D Hypoascorbemia Hypogonadism Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Ichthyosis Idiopathic Avascular Necrosis Indolent Systemic Mastocytosis Infant Gynecomastia Inflammatory Bowel Disease Insulin-Like Growth Factor I Intestinal Disease Irritable Bowel Syndrome Jacobsen Syndrome Joint Disorders Juvenile Primary Osteoporosis Juvenile Rheumatoid Arthritis Kagami-Ogata Syndrome Kashin-Beck Disease Kaufman Oculocerebrofacial Syndrome Labyrinthitis Lactose Intolerance Langerhans Cell Histiocytosis Lathyrism Lepromatous Leprosy Leptin Receptor Deficiency Leukemia Lipid Pneumonia Liver Cirrhosis Liver Disease Loeys-Dietz Syndrome Lung Disease Lupus Erythematosus Lymphangiectasis Lymphoblastic Leukemia Lymphoma Lysinuric Protein Intolerance Macular Dystrophy, Vitelliform, 2 Malignant Spiradenoma Mast Cell Disease Meester-Loeys Syndrome Metabolic Acidosis Microcephaly Microphthalmia Microtia-Anotia Miller-Dieker Lissencephaly Syndrome Mixed Connective Tissue Disease Moebius Syndrome Multiple Sclerosis Mungan Syndrome Muscular Dystrophy Muscular Dystrophy, Becker Type Myasthenia Gravis Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibromatosis, Type Iv, of Riccardi Neutropenia Norrie Disease Occipital Horn Syndrome Ochronosis Oncocytoma Osgood-Schlatter's Disease Osteitis Fibrosa Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrosis Osteomalacia Osteomyelitis Osteonecrosis Osteonecrosis of the Jaw Osteopetrosis Osteoporosis Osteoporosis, Juvenile Osteoporosis-Pseudoglioma Syndrome Osteoporotic Fracture Otosclerosis Overhydrated Hereditary Stomatocytosis Paget's Disease of Bone Paget Disease of Bone 3 Paine Syndrome Pancreatitis Paraplegia Parietal Foramina Pemphigus Pemphigus Vulgaris Peptic Ulcer Disease Periodontal Disease Periodontitis Pernicious Anemia Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pityriasis Rubra Pilaris Pneumonia Pneumothorax Poliomyelitis Polymyositis Postpartum Depression Prader-Willi Syndrome Pre-Eclampsia Premature Menopause Premature Ovarian Failure 7 Primary Biliary Cholangitis Primary Biliary Cirrhosis Primary Hyperparathyroidism Primary Intestinal Lymphangiectasia Progressive Relapsing Multiple Sclerosis Prostate Cancer Prostatitis Pseudoarthrosis Pseudohypoparathyroidism Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Disease, Chronic Obstructive Pulmonary Emphysema Pycnodysostosis Radiculopathy Recessive Dystrophic Epidermolysis Bullosa Renal Oncocytoma Renal Osteodystrophy Renal Tubular Acidosis Retinal Detachment Retinitis Retinoblastoma Rett Syndrome Rheumatic Disease Rheumatoid Arthritis Rhinitis Rickets Ring Chromosome 2 Sarcoma Satb2-Associated Syndrome Schistosomiasis Schizophrenia Sclerosteosis 1 Scoliosis Sensorineural Hearing Loss Severe Congenital Neutropenia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sickle Cell Anemia Siderosis Silicosis Spasticity Spastic Paraparesis Spinal Cord Injury Spinal Stenosis Splenomegaly Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylolisthesis Spondyloocular Syndrome Spondylosis Stickler Syndrome Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Syncope Synovial Chondromatosis Systemic Lupus Erythematosus Systemic Mastocytosis Tarsal Tunnel Syndrome Taurodontism Temple-Baraitser Syndrome Temporal Arteritis Testicular Cancer Thalassemia Thyroiditis Transsexualism Transsexuality Tropical Spastic Paraparesis Ulcerative Colitis Urticaria Urticaria Pigmentosa Uveitis Vaginitis Vascular Disease Werner Syndrome Xanthomatosis