Most Common Diagnoses from May 01, 2006 to Sep 27, 2026

out of 6251047 cases



ICD Diagnosis Cases
F00.0 Dementia in Alzheimer's disease with early onset (G30.0+) 0
E89.5 Postprocedural testicular hypofunction 0
E89.4 Postprocedural ovarian failure 0
E85.8 Other amyloidosis 0
E85.4 Organ-limited amyloidosis 0
E84.8 Cystic fibrosis with other manifestations 0
E80.3 Defects of catalase and peroxidase 0
E77 Disorders of glycoprotein metabolism 0
E76.8 Other disorders of glucosaminoglycan metabolism 0
E67.2 Megavitamin-B 6 syndrome 0
E61.9 Deficiency of nutrient elements, unspecified 0
E61.7 Deficiency of multiple nutrient elements 0
E59 Dietary selenium deficiency 0
E51.8 Other manifestations of thiamine deficiency 0
E51.1 Beriberi 0
E51 Thiamine deficiency 0
E50.7 Other ocular manifestations of vitamin A deficiency 0
E50.6 Vitamin A deficiency with xerophthalmic scars of cornea 0
E50.5 Vitamin A deficiency with night blindness 0
E50.4 Vitamin A deficiency with keratomalacia 0
E50.3 Vitamin A deficiency with corneal ulceration and xerosis 0
E50.2 Vitamin A deficiency with corneal xerosis 0
E50.1 Vitamin A deficiency with Bitot's spot and conjunctival xerosis 0
E50.0 Vitamin A deficiency with conjunctival xerosis 0
E50 Vitamin A deficiency 0
E35.8* Disorders of other endocrine glands in diseases classified elsewhere 0
E35.8 Disorders of other endocrine glands in diseases classified elsewhere 0
E35.1* Disorders of adrenal glands in diseases classified elsewhere 0
E35.0 Disorders of thyroid gland in diseases classified elsewhere 0
E35* Disorders of endocrine glands in diseases classified elsewhere 0
E34.2 Ectopic hormone secretion, not elsewhere classified 0
E34.1 Other hypersecretion of intestinal hormones 0
E34.0 Carcinoid syndrome 0
E31.9 Polyglandular dysfunction, unspecified 0
E31.8 Other polyglandular dysfunction 0
E28.1 Androgen excess 0
E25.8 Other adrenogenital disorders 0
E24.4 Alcohol-induced pseudo-Cushing's syndrome 0
E24.1 Nelson's syndrome 0
E21.5 Disorder of parathyroid gland, unspecified 0
E21.2 Other hyperparathyroidism 0
E16.4 Abnormal secretion of gastrin 0
E14.5 With peripheral circulatory complications 0
E03.4 Atrophy of thyroid (acquired) 0
E00.2 Congenital iodine-deficiency syndrome, mixed type 0
D86.8 Sarcoidosis of other and combined sites 0
D86.3 Sarcoidosis of skin 0
D84.0 Lymphocyte function antigen-1 [LFA-1] defect 0
D82.2 Immunodeficiency with short-limbed stature 0
D81.7 Major histocompatibility complex class II deficiency 0