Code
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| Description
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|---|---|
E75249
|
Niemann-Pick disease, unspecified
|
E7525
|
Metachromatic leukodystrophy
|
E7526
|
Sulfatase deficiency
|
E7529
|
Other sphingolipidosis
|
E753
|
Sphingolipidosis, unspecified
|
E754
|
Neuronal ceroid lipofuscinosis
|
E755
|
Other lipid storage disorders
|
E756
|
Lipid storage disorder, unspecified
|
E7601
|
Hurler's syndrome
|
E7602
|
Hurler-Scheie syndrome
|
E7603
|
Scheie's syndrome
|
E761
|
Mucopolysaccharidosis, type II
|
E76210
|
Morquio A mucopolysaccharidoses
|
E76211
|
Morquio B mucopolysaccharidoses
|
E76219
|
Morquio mucopolysaccharidoses, unspecified
|
E7622
|
Sanfilippo mucopolysaccharidoses
|
E7629
|
Other mucopolysaccharidoses
|
E763
|
Mucopolysaccharidosis, unspecified
|
E768
|
Other disorders of glucosaminoglycan metabolism
|
E769
|
Glucosaminoglycan metabolism disorder, unspecified
|
E770
|
Defects in post-translational modification of lysosomal enzymes
|
E771
|
Defects in glycoprotein degradation
|
E778
|
Other disorders of glycoprotein metabolism
|
E779
|
Disorder of glycoprotein metabolism, unspecified
|
E7800
|
Pure hypercholesterolemia, unspecified
|
E7801
|
Familial hypercholesterolemia
|
E781
|
Pure hyperglyceridemia
|
E782
|
Mixed hyperlipidemia
|
E783
|
Hyperchylomicronemia
|
E7841
|
Elevated Lipoprotein(a)
|
E7849
|
Other hyperlipidemia
|
E785
|
Hyperlipidemia, unspecified
|
E786
|
Lipoprotein deficiency
|
E7870
|
Disorder of bile acid and cholesterol metabolism, unspecified
|
E7871
|
Barth syndrome
|
E7872
|
Smith-Lemli-Opitz syndrome
|
E7879
|
Other disorders of bile acid and cholesterol metabolism
|
E7881
|
Lipoid dermatoarthritis
|
E7889
|
Other lipoprotein metabolism disorders
|
E789
|
Disorder of lipoprotein metabolism, unspecified
|
E790
|
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
|
E791
|
Lesch-Nyhan syndrome
|
E792
|
Myoadenylate deaminase deficiency
|
E798
|
Other disorders of purine and pyrimidine metabolism
|
E799
|
Disorder of purine and pyrimidine metabolism, unspecified
|
E800
|
Hereditary erythropoietic porphyria
|
E801
|
Porphyria cutanea tarda
|
E8020
|
Unspecified porphyria
|
E8021
|
Acute intermittent (hepatic) porphyria
|
E8029
|
Other porphyria
|
E803
|
Defects of catalase and peroxidase
|
E804
|
Gilbert syndrome
|
E805
|
Crigler-Najjar syndrome
|
E806
|
Other disorders of bilirubin metabolism
|
E807
|
Disorder of bilirubin metabolism, unspecified
|
E8300
|
Disorder of copper metabolism, unspecified
|
E8301
|
Wilson's disease
|
E8309
|
Other disorders of copper metabolism
|
E8310
|
Disorder of iron metabolism, unspecified
|
E83110
|
Hereditary hemochromatosis
|
E83111
|
Hemochromatosis due to repeated red blood cell transfusions
|
E83118
|
Other hemochromatosis
|
E83119
|
Hemochromatosis, unspecified
|
E8319
|
Other disorders of iron metabolism
|
E832
|
Disorders of zinc metabolism
|
E8330
|
Disorder of phosphorus metabolism, unspecified
|
E8331
|
Familial hypophosphatemia
|
E8332
|
Hereditary vitamin D-dependent rickets (type 1) (type 2)
|
E8339
|
Other disorders of phosphorus metabolism
|
E8340
|
Disorders of magnesium metabolism, unspecified
|
E8341
|
Hypermagnesemia
|
E8342
|
Hypomagnesemia
|
E8349
|
Other disorders of magnesium metabolism
|
E8350
|
Unspecified disorder of calcium metabolism
|
E8351
|
Hypocalcemia
|
E8352
|
Hypercalcemia
|
E8359
|
Other disorders of calcium metabolism
|
E8381
|
Hungry bone syndrome
|
E8389
|
Other disorders of mineral metabolism
|
E839
|
Disorder of mineral metabolism, unspecified
|
E840
|
Cystic fibrosis with pulmonary manifestations
|
E8411
|
Meconium ileus in cystic fibrosis
|
E8419
|
Cystic fibrosis with other intestinal manifestations
|
E848
|
Cystic fibrosis with other manifestations
|
E849
|
Cystic fibrosis, unspecified
|
E850
|
Non-neuropathic heredofamilial amyloidosis
|
E851
|
Neuropathic heredofamilial amyloidosis
|
E852
|
Heredofamilial amyloidosis, unspecified
|
E853
|
Secondary systemic amyloidosis
|
E854
|
Organ-limited amyloidosis
|
E8581
|
Light chain (AL) amyloidosis
|
E8582
|
Wild-type transthyretin-related (ATTR) amyloidosis
|
E8589
|
Other amyloidosis
|
E859
|
Amyloidosis, unspecified
|
E860
|
Dehydration
|
E861
|
Hypovolemia
|
E869
|
Volume depletion, unspecified
|
E870
|
Hyperosmolality and hypernatremia
|
E871
|
Hypo-osmolality and hyponatremia
|
E872
|
Acidosis
|
Subsets and Splits
Diabetes Codes E10-E14
The query retrieves and sorts records with "Code" values between 'E10' and 'E14', offering a basic filter of the dataset but not providing significant analytical insights.