Code
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| Description
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|---|---|
E71120
|
Methylmalonic acidemia
|
E71121
|
Propionic acidemia
|
E71128
|
Other disorders of propionate metabolism
|
E7119
|
Other disorders of branched-chain amino-acid metabolism
|
E712
|
Disorder of branched-chain amino-acid metabolism, unspecified
|
E7130
|
Disorder of fatty-acid metabolism, unspecified
|
E71310
|
Long chain/very long chain acyl CoA dehydrogenase deficiency
|
E71311
|
Medium chain acyl CoA dehydrogenase deficiency
|
E71312
|
Short chain acyl CoA dehydrogenase deficiency
|
E71313
|
Glutaric aciduria type II
|
E71314
|
Muscle carnitine palmitoyltransferase deficiency
|
E71318
|
Other disorders of fatty-acid oxidation
|
E7132
|
Disorders of ketone metabolism
|
E7139
|
Other disorders of fatty-acid metabolism
|
E7140
|
Disorder of carnitine metabolism, unspecified
|
E7141
|
Primary carnitine deficiency
|
E7142
|
Carnitine deficiency due to inborn errors of metabolism
|
E7143
|
Iatrogenic carnitine deficiency
|
E71440
|
Ruvalcaba-Myhre-Smith syndrome
|
E71448
|
Other secondary carnitine deficiency
|
E7150
|
Peroxisomal disorder, unspecified
|
E71510
|
Zellweger syndrome
|
E71511
|
Neonatal adrenoleukodystrophy
|
E71518
|
Other disorders of peroxisome biogenesis
|
E71520
|
Childhood cerebral X-linked adrenoleukodystrophy
|
E71521
|
Adolescent X-linked adrenoleukodystrophy
|
E71522
|
Adrenomyeloneuropathy
|
E71528
|
Other X-linked adrenoleukodystrophy
|
E71529
|
X-linked adrenoleukodystrophy, unspecified type
|
E7153
|
Other group 2 peroxisomal disorders
|
E71540
|
Rhizomelic chondrodysplasia punctata
|
E71541
|
Zellweger-like syndrome
|
E71542
|
Other group 3 peroxisomal disorders
|
E71548
|
Other peroxisomal disorders
|
E7200
|
Disorders of amino-acid transport, unspecified
|
E7201
|
Cystinuria
|
E7202
|
Hartnup's disease
|
E7203
|
Lowe's syndrome
|
E7204
|
Cystinosis
|
E7209
|
Other disorders of amino-acid transport
|
E7210
|
Disorders of sulfur-bearing amino-acid metabolism, unspecified
|
E7211
|
Homocystinuria
|
E7212
|
Methylenetetrahydrofolate reductase deficiency
|
E7219
|
Other disorders of sulfur-bearing amino-acid metabolism
|
E7220
|
Disorder of urea cycle metabolism, unspecified
|
E7221
|
Argininemia
|
E7222
|
Arginosuccinic aciduria
|
E7223
|
Citrullinemia
|
E7229
|
Other disorders of urea cycle metabolism
|
E723
|
Disorders of lysine and hydroxylysine metabolism
|
E724
|
Disorders of ornithine metabolism
|
E7250
|
Disorder of glycine metabolism, unspecified
|
E7251
|
Non-ketotic hyperglycinemia
|
E7252
|
Trimethylaminuria
|
E7253
|
Primary hyperoxaluria
|
E7259
|
Other disorders of glycine metabolism
|
E7281
|
Disorders of gamma aminobutyric acid metabolism
|
E7289
|
Other specified disorders of amino-acid metabolism
|
E729
|
Disorder of amino-acid metabolism, unspecified
|
E730
|
Congenital lactase deficiency
|
E731
|
Secondary lactase deficiency
|
E738
|
Other lactose intolerance
|
E739
|
Lactose intolerance, unspecified
|
E7400
|
Glycogen storage disease, unspecified
|
E7401
|
von Gierke disease
|
E7402
|
Pompe disease
|
E7403
|
Cori disease
|
E7404
|
McArdle disease
|
E7409
|
Other glycogen storage disease
|
E7410
|
Disorder of fructose metabolism, unspecified
|
E7411
|
Essential fructosuria
|
E7412
|
Hereditary fructose intolerance
|
E7419
|
Other disorders of fructose metabolism
|
E7420
|
Disorders of galactose metabolism, unspecified
|
E7421
|
Galactosemia
|
E7429
|
Other disorders of galactose metabolism
|
E7431
|
Sucrase-isomaltase deficiency
|
E7439
|
Other disorders of intestinal carbohydrate absorption
|
E744
|
Disorders of pyruvate metabolism and gluconeogenesis
|
E74810
|
Glucose transporter protein type 1 deficiency
|
E74818
|
Other disorders of glucose transport
|
E74819
|
Disorders of glucose transport, unspecified
|
E7489
|
Other specified disorders of carbohydrate metabolism
|
E749
|
Disorder of carbohydrate metabolism, unspecified
|
E7500
|
GM2 gangliosidosis, unspecified
|
E7501
|
Sandhoff disease
|
E7502
|
Tay-Sachs disease
|
E7509
|
Other GM2 gangliosidosis
|
E7510
|
Unspecified gangliosidosis
|
E7511
|
Mucolipidosis IV
|
E7519
|
Other gangliosidosis
|
E7521
|
Fabry (-Anderson) disease
|
E7522
|
Gaucher disease
|
E7523
|
Krabbe disease
|
E75240
|
Niemann-Pick disease type A
|
E75241
|
Niemann-Pick disease type B
|
E75242
|
Niemann-Pick disease type C
|
E75243
|
Niemann-Pick disease type D
|
E75244
|
Niemann-Pick disease type A/B
|
E75248
|
Other Niemann-Pick disease
|
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.