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Nume Congenital Hypothyroidism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Congenital hypothyroidism without goitre; Congenital iodine-deficiency syndrome, myxoedematous type
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli endocrine
Boli din aceeaşi familie Central 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 Acromegaly Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome 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 Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Athyreosis Attention Deficit-Hyperactivity Disorder Autoimmune Disease of Endocrine System Autosomal Recessive Congenital Ichthyosis Beckwith-Wiedemann Syndrome Benign Struma Ovarii Biotinidase Deficiency Blepharophimosis Blood Group--Ahonen Blood Group, Dombrock 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 Brachydactyly Cardiogenic Shock Celiac Disease 1 Central Congenital Hypothyroidism Central Nervous System Disease Cerebellar Hypoplasia Chediak-Higashi Syndrome Choanal Atresia, Posterior Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Cleidocranial Dysplasia Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Hypothyroidism Due to Maternal Intake of Antithyroid Drugs Congenital Hypothyroidism Due to Transplacental Passage of Maternal Tsh-Binding Inhibitory Antibodies Conjunctivitis Craniosynostosis 1 Cutis Marmorata Telangiectatica Congenita Cyclic Neutropenia Cystic Fibrosis Diabetes Mellitus Diencephalic Syndrome Down Syndrome Dwarfism Dyshormonogenic Goiter Dyskeratosis Congenita Endemic Goiter Endotheliitis Epicanthus Esophageal Atresia Familial Thyroid Dyshormonogenesis Fanconi Anemia, Complementation Group E Fetal Iodine Deficiency Disorder Follicular Adenoma Galactosemia Gigantism Goiter Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors Graves' Disease Graves Disease 1 Hashimoto Thyroiditis Hepatic Adenomas, Familial Hepatitis Hirschsprung Disease 2 Homocystinuria Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperphenylalaninemia Hyperthyroidism Hyperthyroxinemia Hypertrichosis Hypertrophic Pyloric Stenosis Hypoganglionosis Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypothyroidism Hypothyroidism, Congenital, Nongoitrous, 2 Hypothyroidism, Congenital, Nongoitrous, 4 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function Hypothyroidism Due to Iodide Transport Defect Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Hypotonia Ichthyosis Infertility Kernicterus Lactocele Laryngeal Cleft Lissencephaly Lung Disease Maple Syrup Urine Disease Megacolon Multinodular Goiter Muscular Atrophy Myxedema Neonatal Diabetes Mellitus Neonatal Hypothyroidism Neonatal Respiratory Failure Neonatal Stroke Neonatal Thyrotoxicosis Nephrocalcinosis Nervous System Disease Neuronitis Nodular Goiter Nontoxic Goiter Osseous Heteroplasia, Progressive Osteopetrosis Ovarian Germ Cell Cancer Ovarian Germ Cell Teratoma Papillary Carcinoma Papillary Thyroid Microcarcinoma Pendred Syndrome Pernicious Anemia Peters-Plus Syndrome Phace Syndrome Phenylketonuria Pierre Robin Syndrome Plummer's Disease Polycystic Kidney Disease Polycystic Kidney Disease 5 Prader-Willi Syndrome Precocious Puberty Premature Menopause Primrose Syndrome Pseudohypoparathyroidism Ptosis Pyloric Stenosis Slipped Capital Femoral Epiphysis Spinal Muscular Atrophy Spindle Cell Hemangioma Struma Ovarii Subacute Lymphocytic Thyroiditis Subacute Thyroiditis Teeth Present at Birth Three M Syndrome 1 Thyroid Cancer Thyroid Cancer, Anaplastic Thyroid Cancer, Nonmedullary, 1 Thyroid Cancer, Nonmedullary, 2 Thyroid Ectopia Thyroid Gland Disease Thyroiditis Townes-Brocks Syndrome Toxic Diffuse Goiter Treacher Collins Syndrome 1 Triple X Syndrome Urinary System Disease Water-Clear Cell Adenoma