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Nume Hypothyroidism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Disorders of thyroid gland in diseases classified elsewhere; Hypothyroidism, unspecified; Other specified disorders of thyroid
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli endocrine
Boli din aceeaşi familie Central Congenital Hypothyroidism; Congenital Hypothyroidism; Congenital Hypothyroidism Due to Maternal Intake of Antithyroid Drugs; Congenital Hypothyroidism Due to Transplacental Passage of Maternal Tsh-Binding Inhibitory Antibodies; Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function; Hypothyroidism Due to Iodide Transport Defect

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Boli A-Z Acanthosis Nigricans Aceruloplasminemia Achalasia Acquired Immunodeficiency Syndrome Acquired Von Willebrand Syndrome Acromegaly Acth Deficiency, Isolated Acute Adrenal Insufficiency Acute Monoblastic Leukemia Acute Myocardial Infarction Adenocarcinoma Adenohypophysitis Adenoma Adenosine Deaminase Deficiency Adrenomyeloneuropathy Adult-Onset Nemaline Myopathy Aging Al Amyloidosis Aland Island Eye Disease Albright's Hereditary Osteodystrophy Alcoholic Hepatitis Alcoholic Liver Cirrhosis Allergic Contact Dermatitis Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Angioedema Aniridia 1 Anorexia Nervosa 1 Anovulation Anterior Compartment Syndrome Anterior Uveitis Aplasia Cutis Congenita Apparent Mineralocorticoid Excess Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Athyreosis Atp8b1 Deficiency Atrial Fibrillation Atrial Standstill Atrioventricular Block Atrophic Gastritis Atrophic Rhinitis Attention Deficit-Hyperactivity Disorder Atypical Lichen Myxedematosus Audiogenic Seizures Autoimmune Disease Autoimmune Disease of Endocrine System Autoimmune Hepatitis Autoimmune Pancreatitis Autoimmune Polyglandular Syndrome Type 3 Autosomal Recessive Congenital Ichthyosis Beckwith-Wiedemann Syndrome Biotinidase Deficiency Bipolar I Disorder Bleeding Disorder, Platelet-Type, 11 Blepharophimosis 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 8 Brachydactyly Brain Injury Breast Cancer Bronchiolitis Bronchiolitis Obliterans Bullous Pemphigoid Burning Mouth Syndrome Burns Camurati-Engelmann Disease Candidiasis Capgras Syndrome Cardiac Tamponade Cardiogenic Shock Carotenemia Carpal Tunnel Syndrome Cat Eye Syndrome Celiac Disease 1 Central Congenital Hypothyroidism Central Nervous System Disease Central Nervous System Vasculitis Central Pontine Myelinolysis Central Sleep Apnea Cerebellar Hypoplasia Cerebritis Cerebrovascular Disease Cervicitis Chediak-Higashi Syndrome Childhood Medulloblastoma Choanal Atresia, Posterior Cholangitis Cholecystitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromophobe Adenoma Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 5q Duplication Chronic Mucocutaneous Candidiasis Chronic Rhinitis Chylothorax, Congenital Cleft Lip Cleidocranial Dysplasia Colitis Collagen Disease Colon Adenocarcinoma Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Hypothyroidism Congenital Nystagmus Congenital Rubella Congestive Heart Failure Conjunctivitis Conn's Syndrome Connective Tissue Disease Constipation Contact Dermatitis Coronary Artery Dissection, Spontaneous Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis Craniosynostosis 1 Cutis Laxa Cutis Marmorata Telangiectatica Congenita Cutis Verticis Gyrata Cyclic Neutropenia Cystadenoma Cystic Fibrosis Cystinosis Dandy-Walker Syndrome Defective Apolipoprotein B-100 Demyelinating Disease Dermatitis Dermatitis Herpetiformis Diabetes Insipidus Diabetes Mellitus Diencephalic Syndrome Differentiated Thyroid Carcinoma Diffuse Lymphatic Malformation Dilated Cardiomyopathy Discoid Lupus Erythematosus Down Syndrome Dwarfism Dyshormonogenic Goiter Dyskeratosis Congenita Eales Disease Eclampsia Ectodermal Dysplasia Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia Ehrlichiosis Elephantiasis Empty Sella Syndrome Encephalitis Encephalopathy Endemic Goiter Endogenous Depression Endotheliitis End Stage Renal Failure Eosinophilic Fasciitis Epicanthus Epilepsy Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Epiphysiolysis of the Hip Erythema Elevatum Diutinum Esophageal Atresia Esophageal Cancer Essential Tremor Euthyroid Sick Syndrome Exophthalmos Fabry Disease Facial Neuralgia Familial Adenomatous Polyposis Familial Mediterranean Fever Familial Thyroid Dyshormonogenesis Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fatty Liver Disease Fibrous Dysplasia Focal Segmental Glomerulosclerosis Follicular Adenoma Foot Drop Friedreich Ataxia 1 Frozen Shoulder Fryns Microphthalmia Syndrome Fucosidosis Fundus Albipunctatus Galactorrhea Galactorrhoea-Hyperprolactinaemia Galactose Epimerase Deficiency Galactosemia Gapo Syndrome Gastric Cancer Gastric Neuroendocrine Tumor Gastritis Gastrointestinal Stromal Tumor Generalized Resistance to Thyroid Hormone Genitopatellar Syndrome Gerstmann Syndrome Gestational Diabetes Gestational Trophoblastic Neoplasm Giardioză Gigantism Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioma Glomerulonephritis Glycogen Storage Disease Goiter Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors Gonadal Dysgenesis Granuloma Annulare Graves' Disease Graves Disease 1 Griscelli Syndrome Growth Hormone Deficiency Gynecomastia Hashimoto Thyroiditis Headache Helicobacter Pylori Infection Hemangioendothelioma Hemangioma Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hidradenitis Hidradenitis Suppurativa Hirschsprung Disease 2 Histiocytosis Homocystinuria Horseshoe Kidney Human Coronavirus Sensitivity Hunter-Mcalpine Syndrome Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hyperparathyroidism Hyperphenylalaninemia Hyperprolactinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hyperthyroxinemia Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hyperuricemia Hypoadrenalism Hypoaldosteronism Hypoganglionosis Hypogonadism Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypothyroidism, Central, and Testicular Enlargement Hypothyroidism, Congenital, Nongoitrous, 1 Hypothyroidism, Congenital, Nongoitrous, 2 Hypothyroidism, Congenital, Nongoitrous, 4 Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Hypotonia Ichthyosis Idiopathic Hypersomnia Idiopathic Pleuroparenchymal Fibroelastosis Igg4-Related Thyroid Disease Immune-Complex Glomerulonephritis Immunoglobulin Alpha Deficiency Infant Gynecomastia Infertility Inflammatory Bowel Disease Insulin-Like Growth Factor I Interatrial Communication Internuclear Ophthalmoplegia Interstitial Keratitis Intracranial Hypertension Ischemia Isolated Cleft Lip Jacobsen Syndrome Juvenile Rheumatoid Arthritis Kearns-Sayre Syndrome Keratoconjunctivitis Keratoconjunctivitis Sicca Kernicterus Kidney Cancer Kikuchi Disease Kocher-Debre-Semelaigne Syndrome Lactic Acidosis Lactocele Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Laron Syndrome Laryngeal Cleft Laryngitis Lateral Sinus Thrombosis Left Ventricular Noncompaction Lesch-Nyhan Syndrome Leukemia Lichen Planus Lichen Sclerosus Lipoid Nephrosis Lissencephaly Lissencephaly 1 Liver Cirrhosis Liver Disease Localized Scleroderma Lung Cancer Lung Disease Lupus Erythematosus Lymphangitis Lymphoblastic Leukemia Lymphocytic Hypophysitis Lymphoma Lymphomatous Thyroiditis Macrocytic Anemia Macroglossia Macular Amyloidosis Major Affective Disorder 2 Male Infertility Maple Syrup Urine Disease Mccune-Albright Syndrome Medulloblastoma Megacolon Megaloblastic Anemia Melanoma Meningitis Meningococcal Meningitis Meralgia Paresthetica Metabolic Acidosis Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mixed Connective Tissue Disease Mononeuropathy of the Median Nerve, Mild Morbid Obesity Moyamoya Disease 1 Mucinoses Mucopolysaccharidosis, Type Vii Mucosal Melanoma Mucositis Multidrug-Resistant Tuberculosis Multinodular Goiter Multiple Cranial Nerve Palsy Multiple Sclerosis Muscular Atrophy Musical Perfect Pitch Myasthenia Gravis Myocardial Infarction Myopathy Myotonia Myotonia Congenita Myotonic Dystrophy Myxedema Nasopharyngeal Carcinoma Nasopharyngitis Necrobiosis Lipoidica Necrotizing Fasciitis Nemaline Myopathy Neonatal Diabetes Mellitus Neonatal Hypothyroidism Neonatal Respiratory Failure Neonatal Stroke Neonatal Thyrotoxicosis Nephrocalcinosis Nephrogenic Systemic Fibrosis Nephrotic Syndrome Nervous System Disease Netherton Syndrome Neuritis Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuromuscular Disease Neuronitis Neuropathy Neutropenia Neutrophil Actin Dysfunction Nevus Comedonicus New Daily-Persistent Headache Nodular Goiter Nontoxic Goiter Occipital Horn Syndrome Ocular Motor Apraxia Ohdo Syndrome Omphalocele Open-Angle Glaucoma Optic Nerve Hypoplasia, Bilateral Optic Neuritis Oral Lichen Planus Osseous Heteroplasia, Progressive Osteomalacia Osteopetrosis Ovarian Cyst Ovarian Hyperstimulation Syndrome Overhydrated Hereditary Stomatocytosis Pancreatitis Pancytopenia Papillary Carcinoma Papillary Thyroid Microcarcinoma Papular Mucinosis Paralytic Ileus Parathyroid Adenoma Parathyroid Carcinoma Pemphigus Pemphigus Vulgaris Pendred Syndrome Pericardial Effusion Peripartum Cardiomyopathy Peritonitis Pernicious Anemia Peters-Plus Syndrome Phace Syndrome Phenylketonuria Pierre Robin Syndrome Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Pityriasis Rubra Pilaris Placental Abruption Plummer's Disease Pneumonia Polycystic Kidney Disease Polycystic Kidney Disease 5 Polycystic Ovary Syndrome Polycythemia Polyhydramnios Polymyositis Polyneuropathy Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Porphyria Porphyria Cutanea Tarda Portal Hypertension Posterior Scleritis Postpoliomyelitis Syndrome Postsurgical Hypothyroidism Prader-Willi Syndrome Precocious Puberty Prediabetes Syndrome Pre-Eclampsia Premature Ovarian Failure 7 Primary Biliary Cholangitis Primary Hyperoxaluria Primary Hyperparathyroidism Primrose Syndrome Prostatitis Protein-Losing Enteropathy Proteus Syndrome Pseudohermaphroditism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Pseudomyotonia Psoriasis Psoriasis 13 Pten Hamartoma Tumor Syndrome Ptosis Pulmonary Edema Pulmonary Hypertension Pulmonary Hypertension, Neonatal Pulmonary Hypertension, Primary, 1 Pure Red-Cell Aplasia Purpura Pyloric Stenosis Quadriplegia Renal Hypoplasia Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Retroperitoneal Fibrosis Rheumatic Disease Rheumatoid Arthritis Rhinitis Ring Chromosome 13 Ring Chromosome 18 Ringed Hair Rosai-Dorfman Disease Rubella Salt and Pepper Developmental Regression Syndrome Sapho Syndrome Sarcoidosis 2 Satb2-Associated Syndrome Schinzel Giedion Syndrome Schizophrenia Scleritis Secondary Adrenal Insufficiency Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Sertoli Cell Tumor Severe Combined Immunodeficiency Shapiro Syndrome Simpson-Golabi-Behmel Syndrome Sleep Apnea Sleep Disorder Slipped Capital Femoral Epiphysis Smith-Lemli-Opitz Syndrome Spinal Muscular Atrophy Spindle Cell Hemangioma Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Sporotrichosis Squamous Cell Carcinoma Struma Ovarii Sturge-Weber Syndrome Subacute Lymphocytic Thyroiditis Subacute Thyroiditis Suppurative Thyroiditis Syncope Syndrome of Inappropriate Antidiuretic Hormone Systemic Lupus Erythematosus Systolic Heart Failure Tardive Dyskinesia Tarsal Tunnel Syndrome Teeth Present at Birth Temple-Baraitser Syndrome Temporal Arteritis Testicular Disease Tetralogy of Fallot Thalassemia Three M Syndrome 1 Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Thyroglossal Duct Cyst, Familial Thyroid Cancer Thyroid Cancer, Anaplastic Thyroid Cancer, Nonmedullary, 1 Thyroid Cancer, Nonmedullary, 2 Thyroid Crisis Thyroid Dyshormonogenesis 4 Thyroid Ectopia Thyroid Gland Disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant Thyroiditis Thyroid Lymphoma Thyrotropin-Releasing Hormone Deficiency Tooth Agenesis Townes-Brocks Syndrome Toxic Diffuse Goiter Toxoplasmoză Transient Cerebral Ischemia Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor Triple X Syndrome Trophoblastic Neoplasm Tsh Producing Pituitary Tumor Tuberous Sclerosis Turner Syndrome Type 1 Diabetes Mellitus 12 Ulcerative Colitis Urinary System Disease Urticaria Uveitis Vascular Disease Vasculitis Vestibular Disease Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Weaver Syndrome Weber Syndrome Whim Syndrome Williams-Beuren Syndrome Zygomycosis