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Iodine-deficiency-related diffuse goiter (E01.000x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being
Iodine-deficiency-related diffuse (endemic) goiter (E01.000) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is
Cretinism (E00.901) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Sporadic cretinism (E00.900x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Endemic cretinism is congenital disorder from severe maternal/fetal iodine deficiency in endemic goiter regions: neurologic type (mental retardation, deaf-mutism, spastic diplegia) or myxedematous type (hypothyroidism, growth retardation).
内分泌科Congenital iodine-deficiency hypothyroidism (E00.900x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is be
Cretinism (E00.900x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Congenital iodine-deficiency syndrome (E00.900) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compil
Mixed-type endemic cretinism (E00.200x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Mixed-type congenital iodine-deficiency syndrome (E00.200x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction
Congenital iodine-deficiency syndrome, mixed type (E00.200) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is
Hypothyroid endemic cretinism (E00.100x003) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Myxedematous-type endemic cretinism (E00.100x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being comp
Myxedematous-type congenital iodine-deficiency syndrome (E00.100x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introd
Congenital iodine-deficiency syndrome, myxedematous type (E00.100) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduct
Neurologic-type endemic cretinism (E00.000x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compil
Neurologic-type congenital iodine-deficiency syndrome (E00.000x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduc
Congenital iodine-deficiency syndrome, neurologic type (E00.000) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introductio
Cervical lymph node TB (luoli in TCM). Bacilli usually enter from the mouth (carious teeth) or tonsils, with no visible lesion at the entry site; a few are secondary to pulmonary/bronchial TB. It mainly presents as local cold abscesses, with few systemic
内分泌科Diagnosis and treatment of diabetes, thyroid diseases, gout, dyslipidemia and various metabolic diseases, providing refined blood glucose management and endocrine regulation.
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