| C0000731 |
BXGD000002 |
Abdomen distended |
Digestive System Diseases |
| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001624 |
BXGD000067 |
Adrenal Gland Neoplasms |
Neoplasms; Endocrine System Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002793 |
BXGD000130 |
Anaplasia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0004135 |
BXGD000257 |
Ataxia Telangiectasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0006905 |
BXGD000419 |
Capillary Fragility |
|
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007115 |
BXGD000432 |
Malignant neoplasm of thyroid |
Neoplasms; Endocrine System Diseases |
| C0007133 |
BXGD000442 |
Carcinoma, Papillary |
Neoplasms |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0007682 |
BXGD000471 |
CNS disorder |
Nervous System Diseases |
| C0007867 |
BXGD000497 |
Cervix Diseases |
Female Urogenital Diseases and Pregnancy Complications |
| C0009806 |
BXGD000633 |
Constipation |
Pathological Conditions, Signs and Symptoms |
| C0010308 |
BXGD000661 |
Congenital Hypothyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011854 |
BXGD000753 |
Diabetes Mellitus, Insulin-Dependent |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0011991 |
BXGD000766 |
Diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0015300 |
BXGD000973 |
Exophthalmos |
Eye Diseases |
| C0015397 |
BXGD000983 |
Disorder of eye |
Eye Diseases |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0016053 |
BXGD001041 |
Fibromyalgia |
Musculoskeletal Diseases; Nervous System Diseases |
| C0018021 |
BXGD001162 |
Goiter |
Endocrine System Diseases |
| C0018023 |
BXGD001164 |
Nodular Goiter |
Endocrine System Diseases |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018798 |
BXGD001223 |
Congenital Heart Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0020450 |
BXGD001388 |
Hyperemesis Gravidarum |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020550 |
BXGD001429 |
Hyperthyroidism |
Endocrine System Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0023487 |
BXGD001669 |
Acute Promyelocytic Leukemia |
Neoplasms |
| C0024121 |
BXGD001735 |
Lung Neoplasms |
Neoplasms; Respiratory Tract Diseases |
| C0024232 |
BXGD001751 |
Lymphatic Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0024421 |
BXGD001770 |
Macroglossia |
Stomatognathic Diseases |
| C0025362 |
BXGD001866 |
Mental Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0026267 |
BXGD001896 |
Mitral Valve Prolapse Syndrome |
Cardiovascular Diseases |
| C0026764 |
BXGD001928 |
Multiple Myeloma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0027121 |
BXGD001973 |
Myositis |
Musculoskeletal Diseases; Nervous System Diseases |
| C0027145 |
BXGD001978 |
Myxedema |
Skin and Connective Tissue Diseases; Endocrine System Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028259 |
BXGD002073 |
Nodule |
|
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029132 |
BXGD002117 |
Disorder of the optic nerve |
Eye Diseases; Nervous System Diseases |
| C0029182 |
BXGD002121 |
orbit (eye disorders) |
Eye Diseases |
| C0029434 |
BXGD002146 |
Osteogenesis Imperfecta |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0033103 |
BXGD002395 |
Pretibial myxedema |
Skin and Connective Tissue Diseases; Endocrine System Diseases |
| C0033844 |
BXGD002435 |
Pseudotumor |
Pathological Conditions, Signs and Symptoms |
| C0034013 |
BXGD002450 |
Precocious Puberty |
Endocrine System Diseases |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036857 |
BXGD002638 |
Severe intellectual disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
Skin and Connective Tissue Diseases |
| C0037284 |
BXGD002679 |
Skin lesion |
Skin and Connective Tissue Diseases |
| C0037317 |
BXGD002689 |
Sleep disturbances |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0038379 |
BXGD002752 |
Strabismus |
Eye Diseases; Nervous System Diseases |
| C0039231 |
BXGD002799 |
Tachycardia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0040021 |
BXGD002834 |
Thromboangiitis Obliterans |
Cardiovascular Diseases |
| C0040115 |
BXGD002841 |
Thymus Hyperplasia |
Hemic and Lymphatic Diseases |
| C0040127 |
BXGD002843 |
Thyroid Crisis |
Endocrine System Diseases |
| C0040128 |
BXGD002844 |
Thyroid Diseases |
Endocrine System Diseases |
| C0040136 |
BXGD002845 |
Thyroid Neoplasm |
Neoplasms; Endocrine System Diseases |
| C0040137 |
BXGD002846 |
Thyroid Nodule |
Neoplasms; Endocrine System Diseases |
| C0040147 |
BXGD002847 |
Thyroiditis |
Endocrine System Diseases |
| C0040149 |
BXGD002848 |
Subacute thyroiditis |
Endocrine System Diseases |
| C0040156 |
BXGD002849 |
Thyrotoxicosis |
Endocrine System Diseases |
| C0041408 |
BXGD002923 |
Turner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0085278 |
BXGD003150 |
Antiphospholipid Syndrome |
Immune System Diseases |
| C0085409 |
BXGD003168 |
Polyendocrinopathies, Autoimmune |
Immune System Diseases; Endocrine System Diseases |
| C0085631 |
BXGD003214 |
Agitation |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0086692 |
BXGD003306 |
Benign Neoplasm |
Neoplasms |
| C0151468 |
BXGD003424 |
Thyroid Gland Follicular Adenoma |
Neoplasms; Endocrine System Diseases |
| C0151514 |
BXGD003429 |
Atrophic condition of skin |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0151516 |
BXGD003430 |
Thyroid Hypoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C0151526 |
BXGD003432 |
Premature Birth |
Female Urogenital Diseases and Pregnancy Complications |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0151908 |
BXGD003502 |
Dry skin |
Skin and Connective Tissue Diseases |
| C0152226 |
BXGD003562 |
Lagophthalmos |
Eye Diseases |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0154143 |
BXGD003704 |
Toxic multinodular goiter |
Endocrine System Diseases |
| C0158983 |
BXGD003915 |
Neonatal thyrotoxicosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C0162538 |
BXGD003954 |
Immunoglobulin A deficiency (disorder) |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0178468 |
BXGD004029 |
Autoimmune thyroid disease |
Immune System Diseases; Endocrine System Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0202239 |
BXGD004087 |
Uric acid measurement (procedure) |
|
| C0205642 |
BXGD004094 |
Adenocarcinoma, Oxyphilic |
Neoplasms |
| C0205646 |
BXGD004098 |
Adenoma, Basal Cell |
Neoplasms |
| C0205647 |
BXGD004099 |
Follicular adenoma |
Neoplasms |
| C0205648 |
BXGD004100 |
Adenoma, Microcystic |
Neoplasms |
| C0205649 |
BXGD004101 |
Adenoma, Monomorphic |
Neoplasms |
| C0205650 |
BXGD004102 |
Papillary adenoma |
Neoplasms |
| C0205651 |
BXGD004103 |
Adenoma, Trabecular |
Neoplasms |
| C0205696 |
BXGD004107 |
Anaplastic carcinoma |
Neoplasms |
| C0205697 |
BXGD004108 |
Carcinoma, Spindle-Cell |
Neoplasms |
| C0205698 |
BXGD004109 |
Undifferentiated carcinoma |
Neoplasms |
| C0205699 |
BXGD004110 |
Carcinomatosis |
Neoplasms |
| C0206139 |
BXGD004159 |
Lichen Planus, Oral |
Skin and Connective Tissue Diseases; Stomatognathic Diseases |
| C0206682 |
BXGD004237 |
Follicular thyroid carcinoma |
Neoplasms |
| C0206693 |
BXGD004244 |
Medullary carcinoma |
Neoplasms |
| C0221232 |
BXGD004413 |
Welts |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases |
| C0232466 |
BXGD004543 |
Feeding difficulties |
|
| C0235991 |
BXGD004802 |
Small for gestational age (disorder) |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications |
| C0238185 |
BXGD004889 |
Juvenile myxedema |
Skin and Connective Tissue Diseases; Endocrine System Diseases |
| C0238461 |
BXGD004936 |
Anaplastic thyroid carcinoma |
Neoplasms |
| C0238462 |
BXGD004937 |
Medullary carcinoma of thyroid |
Neoplasms; Endocrine System Diseases |
| C0238463 |
BXGD004938 |
Papillary thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0239842 |
BXGD005001 |
Tremor of hands |
|
| C0241910 |
BXGD005123 |
Autoimmune Chronic Hepatitis |
Digestive System Diseases; Immune System Diseases |
| C0242292 |
BXGD005146 |
McCune-Albright Syndrome |
Musculoskeletal Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0271742 |
BXGD006254 |
Glucocorticoid deficiency with achalasia |
Digestive System Diseases; Endocrine System Diseases |
| C0271789 |
BXGD006258 |
Hypothyroidism, Congenital, Nongoitrous, 4 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0271790 |
BXGD006259 |
Subclinical hypothyroidism |
Endocrine System Diseases |
| C0271791 |
BXGD006260 |
Severe hypothyroidism |
Endocrine System Diseases |
| C0271814 |
BXGD006263 |
Silent thyroiditis |
Endocrine System Diseases |
| C0271815 |
BXGD006264 |
Postpartum Thyroiditis |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0271829 |
BXGD006267 |
Pendred's syndrome |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0302511 |
BXGD006849 |
Small for gestational age fetus |
Pathological Conditions, Signs and Symptoms |
| C0302840 |
BXGD006855 |
Toxic thyroid adenoma |
Neoplasms; Endocrine System Diseases |
| C0311361 |
BXGD006880 |
Adenomatous goiter |
Neoplasms; Endocrine System Diseases |
| C0339143 |
BXGD007226 |
Thyroid associated opthalmopathies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0342114 |
BXGD007430 |
Diffuse goiter |
Endocrine System Diseases |
| C0342122 |
BXGD007431 |
Toxic diffuse goiter |
Endocrine System Diseases |
| C0342127 |
BXGD007432 |
Toxic nodular goiter |
Endocrine System Diseases |
| C0342136 |
BXGD007433 |
Autonomous thyroid function |
Endocrine System Diseases |
| C0342138 |
BXGD007434 |
Thyrotoxicosis in pregnancy |
Endocrine System Diseases |
| C0342153 |
BXGD007436 |
Congenital thyroid hypoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C0342158 |
BXGD007437 |
Hypothyroidism, Autoimmune |
Immune System Diseases; Endocrine System Diseases |
| C0342162 |
BXGD007438 |
Compensated hypothyroidism |
Endocrine System Diseases |
| C0342190 |
BXGD007440 |
C-cell hyperplasia of thyroid |
Pathological Conditions, Signs and Symptoms; Endocrine System Diseases |
| C0342191 |
BXGD007441 |
Familial dyshormonogenetic goiter |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0342199 |
BXGD007443 |
Iodine deficiency syndrome |
Endocrine System Diseases |
| C0342200 |
BXGD007444 |
Endemic Cretinism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0342208 |
BXGD007445 |
Multinodular goiter |
Neoplasms; Endocrine System Diseases |
| C0342549 |
BXGD007504 |
Familial Testotoxicosis |
Endocrine System Diseases |
| C0349588 |
BXGD007933 |
Short stature |
|
| C0393639 |
BXGD008110 |
Hashimoto's encephalitis |
Nervous System Diseases; Endocrine System Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0424605 |
BXGD008535 |
Developmental delay (disorder) |
Mental Disorders |
| C0454644 |
BXGD008850 |
Delayed speech and language development |
Behavior and Behavior Mechanisms |
| C0456132 |
BXGD008869 |
Large fontanelle |
|
| C0474808 |
BXGD008959 |
Follicular neoplasm |
Neoplasms |
| C0520947 |
BXGD009126 |
Clumsiness - motor delay |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0545053 |
BXGD009323 |
Advanced bone age |
|
| C0549473 |
BXGD009384 |
Thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0578870 |
BXGD009553 |
Chronic idiopathic urticaria |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0586553 |
BXGD009609 |
Raised TSH level |
Endocrine System Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600086 |
BXGD009689 |
Toxic goiter |
Endocrine System Diseases |
| C0677607 |
BXGD009721 |
Hashimoto Disease |
Endocrine System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0686619 |
BXGD009835 |
Secondary malignant neoplasm of lymph node |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0700201 |
BXGD009880 |
Dyssomnias |
Nervous System Diseases; Mental Disorders |
| C0700502 |
BXGD009893 |
Acquired hypothyroidism |
Endocrine System Diseases |
| C0741899 |
BXGD010042 |
Poorly differentiated carcinoma |
|
| C0749420 |
BXGD010216 |
Thyroid Agenesis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C0749424 |
BXGD010217 |
Thyroid Hurthle Cell Carcinoma |
Neoplasms; Endocrine System Diseases |
| C0750887 |
BXGD010240 |
Adrenal Cancer |
Neoplasms; Endocrine System Diseases |
| C0812413 |
BXGD010847 |
Malignant Pleural Mesothelioma |
Neoplasms; Respiratory Tract Diseases |
| C0851578 |
BXGD010925 |
Sleep Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0856120 |
BXGD011093 |
Multiple sclerosis relapse |
|
| C0869147 |
BXGD011304 |
Neonatal hyperthyroidism |
Endocrine System Diseases |
| C0878544 |
BXGD011368 |
Cardiomyopathies |
Cardiovascular Diseases |
| C0917799 |
BXGD011410 |
Hypersomnia |
Nervous System Diseases; Mental Disorders |
| C0920350 |
BXGD011466 |
Autoimmune thyroiditis |
Immune System Diseases; Endocrine System Diseases |
| C0947751 |
BXGD011494 |
Vascular inflammations |
Cardiovascular Diseases |
| C0948192 |
BXGD011514 |
Primary infection NOS |
|
| C1096666 |
BXGD011638 |
Thyroid cancer metastatic |
Neoplasms; Endocrine System Diseases |
| C1112776 |
BXGD011687 |
Thyroid hyperplasia |
|
| C1140680 |
BXGD011718 |
Malignant neoplasm of ovary |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1262091 |
BXGD011867 |
Lymphocytic infiltration |
|
| C1262098 |
BXGD011868 |
Congenital hyperthyroidism |
Endocrine System Diseases |
| C1262477 |
BXGD011882 |
Weight decreased |
Pathological Conditions, Signs and Symptoms |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1290884 |
BXGD012198 |
Inflammatory disorder |
Pathological Conditions, Signs and Symptoms |
| C1304508 |
BXGD012341 |
Spindle cell hemangioma |
Neoplasms |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306503 |
BXGD012363 |
Congenital exomphalos |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1337013 |
BXGD012876 |
Differentiated Thyroid Gland Carcinoma |
|
| C1400126 |
BXGD013010 |
Thyroid hypertrophy |
|
| C1456145 |
BXGD013108 |
Dental caries of smooth surface |
Stomatognathic Diseases |
| C1510502 |
BXGD013175 |
Oxyphilic Adenoma |
Neoplasms |
| C1519670 |
BXGD013241 |
Tumor Angiogenesis |
Pathological Conditions, Signs and Symptoms |
| C1563716 |
BXGD013390 |
Thyroid Dysgenesis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C1578691 |
BXGD013428 |
Myxedema, Congenital |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C1608408 |
BXGD013434 |
Malignant transformation |
|
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1709457 |
BXGD013625 |
Papillary Thyroid Microcarcinoma |
Neoplasms; Endocrine System Diseases |
| C1836706 |
BXGD014153 |
Hyperthyroidism, Nonautoimmune |
Endocrine System Diseases |
| C1845847 |
BXGD014760 |
Coarse facial features |
Pathological Conditions, Signs and Symptoms |
| C1846135 |
BXGD014784 |
Autistic features |
|
| C1853237 |
BXGD015319 |
Isolated cases |
|
| C1854301 |
BXGD015391 |
Motor delay |
Mental Disorders |
| C1857276 |
BXGD015688 |
Trichohepatoenteric Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases |
| C1859592 |
BXGD015912 |
ATRICHIA WITH PAPULAR LESIONS |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1863959 |
BXGD016205 |
Hyperthyroidism, Familial Gestational |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1863960 |
BXGD016206 |
Thyroid Adenoma, Hyperfunctioning |
Endocrine System Diseases |
| C1863961 |
BXGD016207 |
Thyroid Carcinoma With Thyrotoxicosis |
Endocrine System Diseases |
| C1864761 |
BXGD016248 |
Thyroid Hormone Metabolism, Abnormal |
Endocrine System Diseases |
| C1955741 |
BXGD016606 |
Glucocorticoid deficiency |
|
| C1963060 |
BXGD016679 |
Agitation, CTCAE 3.0 |
|
| C1963094 |
BXGD016681 |
Dry Skin, CTCAE |
|
| C1998045 |
BXGD016866 |
Subclinical hyperthyroidism |
Endocrine System Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2315100 |
BXGD017021 |
Pediatric failure to thrive |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders |
| C2678303 |
BXGD017402 |
Hoarse cry |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C2745900 |
BXGD017568 |
Promyelocytic leukemia |
|
| C2747905 |
BXGD017582 |
Destructive thyroiditis |
|
| C2919142 |
BXGD017867 |
Short Stature, CTCAE |
|
| C2931367 |
BXGD018010 |
Thyroid cancer, follicular |
Neoplasms |
| C2939419 |
BXGD018178 |
Secondary Neoplasm |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C2940785 |
BXGD018183 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C2940786 |
BXGD018184 |
Thyroid Hormone Resistance Syndrome |
Endocrine System Diseases |
| C3493776 |
BXGD018955 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C3541994 |
BXGD019100 |
Drug Hypersensitivity Syndrome |
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders |
| C3714618 |
BXGD019417 |
Primary Hyperthyroidism |
Endocrine System Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3715197 |
BXGD019449 |
Primary congenital hypothyroidism |
|
| C3826150 |
BXGD019714 |
Hypothyroidism in children |
|
| C3827793 |
BXGD019739 |
Transient hypothyroxinaemia of prematurity |
|
| C3840565 |
BXGD019797 |
Autoimmune thyroid disease (AITD) |
|
| C3887638 |
BXGD019906 |
Failure to thrive in infant |
Pathological Conditions, Signs and Symptoms |
| C3887709 |
BXGD019918 |
Optic Neuropathy |
Eye Diseases; Nervous System Diseases |
| C4021768 |
BXGD020766 |
Abnormality of metabolism/homeostasis |
|
| C4023188 |
BXGD021140 |
Activating thyroid-stimulating hormone receptor defect |
|
| C4225553 |
BXGD022280 |
THYROID CARCINOMA WITH THYROTOXICOSIS, SOMATIC |
|
| C4302198 |
BXGD022528 |
Familial hyperthyroidism |
Endocrine System Diseases |
| C4316995 |
BXGD022715 |
Primary Hypothyroidism |
Endocrine System Diseases |
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4552855 |
BXGD023528 |
Agitation, CTCAE 5.0 |
|
| C4721555 |
BXGD023755 |
Autoimmune hepatitis |
Digestive System Diseases |
| C4722172 |
BXGD023791 |
Primary differentiated carcinoma of thyroid gland |
|
| C4722330 |
BXGD023801 |
Generalized Thyroid Hormone Resistance |
Endocrine System Diseases |
| C4722488 |
BXGD023805 |
Thyroid Stimulating Hormone Resistance |
|