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Nume Hypoparathyroidism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Hypoparathyroidism, unspecified; Idiopathic hypoparathyroidism
Clasificare anatomică Malacards Boli endocrine
Boli din aceeaşi familie Autoimmune Hypoparathyroidism; Secondary Hypoparathyroidism Due to Impaired Parathormon Secretion

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Boli A-Z Acrodysostosis Acromegaly Acute Myocardial Infarction Adult T-Cell Leukemia Aging Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Anauxetic Dysplasia 1 Aneurysm Angioedema Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Autoimmune Disease Autoimmune Hypoparathyroidism Autoimmune Polyendocrine Syndrome Autoimmune Polyendocrine Syndrome Type 1 Axial Osteomalacia Ayme-Gripp Syndrome Basal Ganglia Calcification Beta-Thalassemia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blount's Disease Body Dysmorphic Disorder Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Remodeling Disease Bornholm Eye Disease Brachydactyly Branchiootic Syndrome 1 Burns Calcinosis Calciphylaxis Candidiasis Capgras Syndrome Cartilage-Hair Hypoplasia Cataract Cayler Cardiofacial Syndrome Celiac Disease 1 Central Nervous System Disease Cerebritis Cervical Dystonia Cervicitis Charge Syndrome Chief Cell Adenoma Chondrodysplasia, Blomstrand Type Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosome 10p Deletion Chronic Inflammatory Demyelinating Polyneuropathy Chronic Mucocutaneous Candidiasis Cohen-Gibson Syndrome Congestive Heart Failure Conotruncal Heart Malformations Craniosynostosis 1 Crouzon Syndrome with Acanthosis Nigricans Cytomegalic Inclusion Disease Dementia Demyelinating Polyneuropathy Dermatitis Diabetes Insipidus Diabetes Mellitus Diffuse Idiopathic Skeletal Hyperostosis Digeorge Syndrome Dilated Cardiomyopathy Dubowitz Syndrome Dysostosis Dystonia Encephalomyopathy Encephalopathy Endotheliitis Epilepsy Exfoliative Dermatitis Extraskeletal Chondroma Familial Hypocalciuric Hypercalcemia Fanconi Anemia, Complementation Group E Fanconi Syndrome Focal Epilepsy Focal Segmental Glomerulosclerosis Giant Cell Myocarditis Glomerulonephritis Goiter Gorlin-Chaudhry-Moss Syndrome Graves' Disease Griscelli Syndrome Growth Hormone Deficiency Hemophagocytic Lymphohistiocytosis, Familial, 1 Hepatitis Hepatitis a Hereditary Angioedema Heterochromia Iridis Hutchinson-Gilford Progeria Syndrome Hypercalcemia, Infantile, 1 Hyperostosis Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypervitaminosis D Hypoaldosteronism Hypocalcemia, Autosomal Dominant 1 Hypocalciuric Hypercalcemia, Familial, Type Ii Hypocalciuric Hypercalcemia, Familial, Type Iii Hypoglycemia Hypogonadism Hypokalemia Hypoparathyroidism, Familial Isolated Hypoparathyroidism-Retardation-Dysmorphism Syndrome Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia, Adult Hypophosphatemia Immune Suppression Impaired Renal Function Disease Impetigo Impetigo Herpetiformis Intestinal Pseudo-Obstruction Invasive Malignant Thymoma Kearns-Sayre Syndrome Kenny-Caffey Syndrome Kenny-Caffey Syndrome, Type 2 Klippel-Feil Syndrome Laryngitis Lateral Sclerosis Leukemia Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Long Qt Syndrome Lupus Erythematosus Lymphangiectasia, Intestinal Lymphoma Marfan Syndrome Meniere Disease Metaphyseal Chondrodysplasia, Jansen Type Migraine with or Without Aura 1 Mineral Metabolism Disease Mitochondrial Encephalomyopathy Mitochondrial Trifunctional Protein Deficiency Mood Disorder Multicentric Carpotarsal Osteolysis Syndrome Multinodular Goiter Multiple Endocrine Neoplasia Multiple System Atrophy 1 Mungan Syndrome Myelofibrosis Myocardial Infarction Myopathy Myositis Myositis Ossificans Myotonia Myotonia Congenita Myxedema Nephrocalcinosis Nervous System Disease Neuropathy Occipital Horn Syndrome Oncogenic Osteomalacia Osseous Heteroplasia, Progressive Osteitis Fibrosa Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrodysplasia Osteomalacia Overhydrated Hereditary Stomatocytosis Pallister-Hall Syndrome Papillary Carcinoma Papilledema Paraneoplastic Syndromes Parathyroid Adenoma Parathyroid Carcinoma Parathyroid Gland Disease Paroxysmal Choreoathetosis Periarthritis Pericardial Effusion Peripheral Dysostosis Pernicious Anemia Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Pityriasis Rubra Pilaris Poems Syndrome Polyneuropathy Portal Hypertension Precocious Puberty Premature Ovarian Failure 7 Primary Hyperparathyroidism Proliferative Glomerulonephritis Protein-Losing Enteropathy Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Psoriasis Psoriasis 13 Pulmonary Alveolar Microlithiasis Pulmonary Tuberculosis Pure Red-Cell Aplasia Pustular Psoriasis Pyle Disease Renal Dysplasia Renal Osteodystrophy Renal Tubular Acidosis Retroperitoneal Fibrosis Rheumatoid Arthritis Rickets Ring Chromosome 18 Sakati Syndrome Sarcoidosis 2 Schizophrenia Sclerosing Hepatic Carcinoma Secondary Hyperparathyroidism of Renal Origin Seizure Disorder Sotos Syndrome 1 Spastic Paraplegia 7, Autosomal Recessive Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Status Epilepticus Steatorrhea Subacute Thyroiditis Syncope Systemic Lupus Erythematosus T Cell Deficiency T-Cell Leukemia Thalassemia Thymoma Thyroid Cancer Thyroiditis Tooth Ankylosis Typhoid Fever Velocardiofacial Syndrome Water-Clear Cell Adenoma