PDX Collection 0534 (continued) |
E71111 | 3-methylglutaconic aciduria |
E71118 | Other branched-chain organic acidurias |
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 |
E7200 | Disorders of amino-acid transport, unspecified |
E7201 | Cystinuria |
E7202 | Hartnup's disease |
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 | Hyperoxaluria |
E7259 | Other disorders of glycine metabolism |
E728 | 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 |
E748 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher 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 |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
E755 | Other lipid storage disorders |
E756 | Lipid storage 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 |
E784 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E8889 | Other specified metabolic disorders |
|
PDX Collection 0535 |
C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
C966 | Unifocal Langerhans-cell histiocytosis |
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 |
E803 | Defects of catalase and peroxidase |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8849 | Other mitochondrial metabolism disorders |
E8889 | Other specified metabolic disorders |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |
|
PDX Collection 0536 |
C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
C966 | Unifocal Langerhans-cell histiocytosis |
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 |
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 |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8849 | Other mitochondrial metabolism disorders |
E8889 | Other specified metabolic disorders |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |
|
PDX Collection 0537 |
E7500 | GM2 gangliosidosis, unspecified |
E7501 | Sandhoff disease |
E7502 | Tay-Sachs disease |
E7509 | Other GM2 gangliosidosis |
E7510 | Unspecified gangliosidosis |
E7511 | Mucolipidosis IV |
E7519 | Other gangliosidosis |
E754 | Neuronal ceroid lipofuscinosis |
F842 | Rett's syndrome |
G132 | Systemic atrophy primarily affecting the central nervous system in myxedema |
G138 | Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
G300 | Alzheimer's disease with early onset |
G301 | Alzheimer's disease with late onset |
G308 | Other Alzheimer's disease |
G309 | Alzheimer's disease, unspecified |
G3101 | Pick's disease |
G3109 | Other frontotemporal dementia |
G311 | Senile degeneration of brain, not elsewhere classified |
G312 | Degeneration of nervous system due to alcohol |
G3181 | Alpers disease |
G3182 | Leigh's disease |
G3184 | Mild cognitive impairment, so stated |
G3185 | Corticobasal degeneration |
G3189 | Other specified degenerative diseases of nervous system |
G319 | Degenerative disease of nervous system, unspecified |
G914 | Hydrocephalus in diseases classified elsewhere |
G94 | Other disorders of brain in diseases classified elsewhere |
|
PDX Collection 0538 |
E7500 | GM2 gangliosidosis, unspecified |
E7501 | Sandhoff disease |
E7502 | Tay-Sachs disease |
E7509 | Other GM2 gangliosidosis |
E7510 | Unspecified gangliosidosis |
E7511 | Mucolipidosis IV |
E7519 | Other gangliosidosis |
E7523 | Krabbe disease |
E7525 | Metachromatic leukodystrophy |
E7529 | Other sphingolipidosis |
E754 | Neuronal ceroid lipofuscinosis |
F842 | Rett's syndrome |
G132 | Systemic atrophy primarily affecting the central nervous system in myxedema |
G138 | Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
G312 | Degeneration of nervous system due to alcohol |
G3181 | Alpers disease |
G3182 | Leigh's disease |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
G914 | Hydrocephalus in diseases classified elsewhere |
G9381 | Temporal sclerosis |
G9389 | Other specified disorders of brain |
G939 | Disorder of brain, unspecified |
G94 | Other disorders of brain in diseases classified elsewhere |
G968 | Other specified disorders of central nervous system |
G969 | Disorder of central nervous system, unspecified |
G980 | Neurogenic arthritis, not elsewhere classified |
G988 | Other disorders of nervous system |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
|
PDX Collection 0539 |
D813 | Adenosine deaminase [ADA] deficiency |
D815 | Purine nucleoside phosphorylase [PNP] deficiency |
D81810 | Biotinidase deficiency |
D841 | Defects in the complement system |
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 |
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 |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E850 | Non-neuropathic heredofamilial amyloidosis |
E859 | Amyloidosis, unspecified |
E8881 | Metabolic syndrome |
|
PDX Collection 0540 |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
Q871 | Congenital malformation syndromes predominantly associated with short stature |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |
Q8740 | Marfan's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
|
PDX Collection 0541 |
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 |
|
PDX Collection 0542 |
E850 | Non-neuropathic heredofamilial amyloidosis |
E851 | Neuropathic heredofamilial amyloidosis |
E852 | Heredofamilial amyloidosis, unspecified |
E853 | Secondary systemic amyloidosis |
E854 | Organ-limited amyloidosis |
E858 | Other amyloidosis |
E859 | Amyloidosis, unspecified |
E8881 | Metabolic syndrome |
|
PDX Collection 0543 |
E860 | Dehydration |
E861 | Hypovolemia |
E869 | Volume depletion, unspecified |
E870 | Hyperosmolality and hypernatremia |
E871 | Hypo-osmolality and hyponatremia |
E872 | Acidosis |
E873 | Alkalosis |
E874 | Mixed disorder of acid-base balance |
E875 | Hyperkalemia |
E876 | Hypokalemia |
E8770 | Fluid overload, unspecified |
E8771 | Transfusion associated circulatory overload |
E8779 | Other fluid overload |
E878 | Other disorders of electrolyte and fluid balance, not elsewhere classified |
|
PDX Collection 0544 |
E0821 | Diabetes mellitus due to underlying condition with diabetic nephropathy |
E0822 | Diabetes mellitus due to underlying condition with diabetic chronic kidney disease |
E0829 | Diabetes mellitus due to underlying condition with other diabetic kidney complication |
E0921 | Drug or chemical induced diabetes mellitus with diabetic nephropathy |
E0922 | Drug or chemical induced diabetes mellitus with diabetic chronic kidney disease |
E0929 | Drug or chemical induced diabetes mellitus with other diabetic kidney complication |
E883 | Tumor lysis syndrome |
N000 | Acute nephritic syndrome with minor glomerular abnormality |
N001 | Acute nephritic syndrome with focal and segmental glomerular lesions |
N002 | Acute nephritic syndrome with diffuse membranous glomerulonephritis |
N003 | Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N004 | Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N005 | Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N006 | Acute nephritic syndrome with dense deposit disease |
N007 | Acute nephritic syndrome with diffuse crescentic glomerulonephritis |
N008 | Acute nephritic syndrome with other morphologic changes |
N009 | Acute nephritic syndrome with unspecified morphologic changes |
N010 | Rapidly progressive nephritic syndrome with minor glomerular abnormality |
N011 | Rapidly progressive nephritic syndrome with focal and segmental glomerular lesions |
N012 | Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis |
N013 | Rapidly progressive nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N014 | Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N015 | Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N016 | Rapidly progressive nephritic syndrome with dense deposit disease |
N017 | Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis |
N018 | Rapidly progressive nephritic syndrome with other morphologic changes |
N019 | Rapidly progressive nephritic syndrome with unspecified morphologic changes |
N028 | Recurrent and persistent hematuria with other morphologic changes |
N029 | Recurrent and persistent hematuria with unspecified morphologic changes |
N047 | Nephrotic syndrome with diffuse crescentic glomerulonephritis |
N048 | Nephrotic syndrome with other morphologic changes |
N049 | Nephrotic syndrome with unspecified morphologic changes |
N050 | Unspecified nephritic syndrome with minor glomerular abnormality |
N051 | Unspecified nephritic syndrome with focal and segmental glomerular lesions |
N056 | Unspecified nephritic syndrome with dense deposit disease |
N057 | Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis |
N058 | Unspecified nephritic syndrome with other morphologic changes |
N059 | Unspecified nephritic syndrome with unspecified morphologic changes |
N060 | Isolated proteinuria with minor glomerular abnormality |
N061 | Isolated proteinuria with focal and segmental glomerular lesions |
N066 | Isolated proteinuria with dense deposit disease |
N067 | Isolated proteinuria with diffuse crescentic glomerulonephritis |
N068 | Isolated proteinuria with other morphologic lesion |
N069 | Isolated proteinuria with unspecified morphologic lesion |
N070 | Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality |
N071 | Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions |
N076 | Hereditary nephropathy, not elsewhere classified with dense deposit disease |
N077 | Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis |
N078 | Hereditary nephropathy, not elsewhere classified with other morphologic lesions |
N079 | Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions |
N08 | Glomerular disorders in diseases classified elsewhere |
N140 | Analgesic nephropathy |
N141 | Nephropathy induced by other drugs, medicaments and biological substances |
N142 | Nephropathy induced by unspecified drug, medicament or biological substance |
N143 | Nephropathy induced by heavy metals |
N144 | Toxic nephropathy, not elsewhere classified |
N150 | Balkan nephropathy |
N158 | Other specified renal tubulo-interstitial diseases |
N159 | Renal tubulo-interstitial disease, unspecified |
N16 | Renal tubulo-interstitial disorders in diseases classified elsewhere |
N170 | Acute kidney failure with tubular necrosis |
N171 | Acute kidney failure with acute cortical necrosis |
N172 | Acute kidney failure with medullary necrosis |
N178 | Other acute kidney failure |
N179 | Acute kidney failure, unspecified |
|
PDX Collection 0545 |
C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
C966 | Unifocal Langerhans-cell histiocytosis |
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 |
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 |
E8889 | Other specified metabolic disorders |
|
PDX Collection 0546 |
E368 | Other intraoperative complications of endocrine system |
E89810 | Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure |
E89811 | Postprocedural hemorrhage of an endocrine system organ or structure following other procedure |
E89820 | Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure |
E89821 | Postprocedural hematoma of an endocrine system organ or structure following other procedure |
E89822 | Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure |
E89823 | Postprocedural seroma of an endocrine system organ or structure following other procedure |
E8989 | Other postprocedural endocrine and metabolic complications and disorders |
H95811 | Postprocedural stenosis of right external ear canal |
H95812 | Postprocedural stenosis of left external ear canal |
H95813 | Postprocedural stenosis of external ear canal, bilateral |
H95819 | Postprocedural stenosis of unspecified external ear canal |
H9588 | Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified |
H9589 | Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified |
I973 | Postprocedural hypertension |
M9689 | Other intraoperative and postprocedural complications and disorders of the musculoskeletal system |
N981 | Hyperstimulation of ovaries |
N982 | Complications of attempted introduction of fertilized ovum following in vitro fertilization |
N983 | Complications of attempted introduction of embryo in embryo transfer |
N988 | Other complications associated with artificial fertilization |
N989 | Complication associated with artificial fertilization, unspecified |