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Boli A-Z Acrodysostosis Acute Pancreatitis Albright's Hereditary Osteodystrophy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Axial Osteomalacia Basal Cell Nevus Syndrome Basal Ganglia Calcification Beckwith-Wiedemann Syndrome Behr Syndrome Bipolar Disorder Blepharospasm Blood Group--Ahonen 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Calcinosis Capgras Syndrome Cataract Cerebellar Astrocytoma Cerebritis Cerebrovascular Disease Chiari Malformation Chiari Malformation Type I Chondrodysplasia, Blomstrand Type Choroiditis Clear Cell Adenoma Cohen-Gibson Syndrome Congenital Hypothyroidism Congestive Heart Failure Craniosynostosis Cri-Du-Chat Syndrome Dementia Diabetes Insipidus Diabetes Mellitus Diarrhea Duane Retraction Syndrome 1 Dysostosis Dystonia Empty Sella Syndrome Epilepsy Evans' Syndrome Extraskeletal Chondroma Fanconi Anemia, Complementation Group E Fibrous Dysplasia Focal Epilepsy Fucosidosis Gerstmann Syndrome Gitelman Syndrome Glucocorticoid Resistance, Generalized Glucose Transporter Type 1 Deficiency Syndrome Graves' Disease Griscelli Syndrome Growth Hormone Deficiency Hemochromatosis, Neonatal Hepatic Adenomas, Familial Hereditary Multiple Exostoses Hypercalcemia, Infantile, 1 Hyperostosis Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoaldosteronism Hypoglycemia Hypoparathyroidism Hypophosphatasia, Adult Hypophosphatemia Hypopituitarism Hypothyroidism, Congenital, Nongoitrous, 1 Impaired Renal Function Disease Invasive Malignant Thymoma Juvenile Hereditary Hemochromatosis Juxtacortical Chondroma Laryngeal Cleft Lissencephaly, X-Linked, 1 Lupus Erythematosus Mccune-Albright Syndrome Metal Metabolism Disorder Metaphyseal Chondrodysplasia, Jansen Type Morbid Obesity Multicentric Carpotarsal Osteolysis Syndrome Multiple Enchondromatosis, Maffucci Type Myopathy Myositis Myositis Ossificans Occipital Horn Syndrome Oncogenic Osteomalacia Osseous Heteroplasia, Progressive Osteitis Fibrosa Osteochondrodysplasia Osteomalacia Osteopetrosis Overhydrated Hereditary Stomatocytosis Pancreatitis Parathyroid Adenoma Parathyroid Gland Disease Phelan-Mcdermid Syndrome Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Primary Hyperparathyroidism Primary Hypomagnesemia Pseudohypoparathyroidism, Type Ia Pseudohypoparathyroidism, Type Ib Pseudohypoparathyroidism, Type Ic Pseudohypoparathyroidism, Type Ii Pseudopseudohypoparathyroidism Psoriasis Psoriasis 13 Pyle Disease Renal Osteodystrophy Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Rickets Sclerosing Hepatic Carcinoma Secondary Hyperparathyroidism of Renal Origin Seizure Disorder Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Atrophy Sleep Apnea Slipped Capital Femoral Epiphysis Spinal Stenosis Spondyloarthropathy Steatorrhea Supernumerary Der(22)t(8 Syncope Systemic Lupus Erythematosus Teeth Present at Birth Testotoxicosis Thyroiditis Tooth Ankylosis Turner Syndrome