PDX Collection 0535 (continued) |
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 |
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 |
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 neurocognitive disorder |
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 of uncertain or unknown etiology |
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 |
E7526 | Sulfatase deficiency |
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 |
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 |
D8130 | Adenosine deaminase deficiency, unspecified |
D8131 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
D8132 | Adenosine deaminase 2 deficiency |
D8139 | Other adenosine deaminase 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 |
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 |
E8581 | Light chain (AL) amyloidosis |
E8582 | Wild-type transthyretin-related (ATTR) amyloidosis |
E8589 | Other amyloidosis |
E859 | Amyloidosis, unspecified |
E8881 | Metabolic syndrome |
|
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 |
H49819 | Kearns-Sayre syndrome, unspecified eye |
|
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 |
T8182XA | Emphysema (subcutaneous) resulting from a procedure, initial encounter |
T8189XA | Other complications of procedures, not elsewhere classified, initial encounter |
T819XXA | Unspecified complication of procedure, initial encounter |
|
PDX Collection 0549 |
F05 | Delirium due to known physiological condition |
R45851 | Suicidal ideations |
|
PDX Collection 0553 |
F3113 | Bipolar disorder, current episode manic without psychotic features, severe |
F312 | Bipolar disorder, current episode manic severe with psychotic features |
F3163 | Bipolar disorder, current episode mixed, severe, without psychotic features |
F3164 | Bipolar disorder, current episode mixed, severe, with psychotic features |
|
PDX Collection 0554 |
F3113 | Bipolar disorder, current episode manic without psychotic features, severe |
F312 | Bipolar disorder, current episode manic severe with psychotic features |
F314 | Bipolar disorder, current episode depressed, severe, without psychotic features |
F315 | Bipolar disorder, current episode depressed, severe, with psychotic features |
F3163 | Bipolar disorder, current episode mixed, severe, without psychotic features |
F3164 | Bipolar disorder, current episode mixed, severe, with psychotic features |
|
PDX Collection 0556 |
F459 | Somatoform disorder, unspecified |
F5000 | Anorexia nervosa, unspecified |
F5001 | Anorexia nervosa, restricting type |
F5002 | Anorexia nervosa, binge eating/purging type |
F502 | Bulimia nervosa |
F5081 | Binge eating disorder |
F5082 | Avoidant/restrictive food intake disorder |
F5089 | Other specified eating disorder |
F509 | Eating disorder, unspecified |
F59 | Unspecified behavioral syndromes associated with physiological disturbances and physical factors |
F9821 | Rumination disorder of infancy |
F9829 | Other feeding disorders of infancy and early childhood |
F983 | Pica of infancy and childhood |
|
PDX Collection 0557 |
F5000 | Anorexia nervosa, unspecified |
F5001 | Anorexia nervosa, restricting type |
F5002 | Anorexia nervosa, binge eating/purging type |
F502 | Bulimia nervosa |
F5081 | Binge eating disorder |
F5082 | Avoidant/restrictive food intake disorder |
F5089 | Other specified eating disorder |
F509 | Eating disorder, unspecified |
F9821 | Rumination disorder of infancy |
F9829 | Other feeding disorders of infancy and early childhood |
|
PDX Collection 0558 |
F72 | Severe intellectual disabilities |
F73 | Profound intellectual disabilities |
|
PDX Collection 0559 |
A0221 | Salmonella meningitis |
A170 | Tuberculous meningitis |
A171 | Meningeal tuberculoma |
A2781 | Aseptic meningitis in leptospirosis |
A390 | Meningococcal meningitis |
A5041 | Late congenital syphilitic meningitis |
A5141 | Secondary syphilitic meningitis |
A5213 | Late syphilitic meningitis |
A5482 | Gonococcal brain abscess |
A5484 | Gonococcal pneumonia |
A5489 | Other gonococcal infections |
A549 | Gonococcal infection, unspecified |
A870 | Enteroviral meningitis |
A871 | Adenoviral meningitis |
A872 | Lymphocytic choriomeningitis |
A878 | Other viral meningitis |
A879 | Viral meningitis, unspecified |
B003 | Herpesviral meningitis |
B021 | Zoster meningitis |
B261 | Mumps meningitis |
B375 | Candidal meningitis |
B384 | Coccidioidomycosis meningitis |
B451 | Cerebral cryptococcosis |
B582 | Toxoplasma meningoencephalitis |
G000 | Hemophilus meningitis |
G001 | Pneumococcal meningitis |
G002 | Streptococcal meningitis |
G003 | Staphylococcal meningitis |
G008 | Other bacterial meningitis |
G009 | Bacterial meningitis, unspecified |
G01 | Meningitis in bacterial diseases classified elsewhere |
G02 | Meningitis in other infectious and parasitic diseases classified elsewhere |
G030 | Nonpyogenic meningitis |
G031 | Chronic meningitis |
G032 | Benign recurrent meningitis [Mollaret] |
G038 | Meningitis due to other specified causes |
G039 | Meningitis, unspecified |
G042 | Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
G610 | Guillain-Barre syndrome |
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 0560 |
A0221 | Salmonella meningitis |
A170 | Tuberculous meningitis |
A171 | Meningeal tuberculoma |
A1782 | Tuberculous meningoencephalitis |
A2781 | Aseptic meningitis in leptospirosis |
A390 | Meningococcal meningitis |
A5041 | Late congenital syphilitic meningitis |
A5042 | Late congenital syphilitic encephalitis |
A5141 | Secondary syphilitic meningitis |
A5213 | Late syphilitic meningitis |
A5214 | Late syphilitic encephalitis |
A5482 | Gonococcal brain abscess |
A5484 | Gonococcal pneumonia |
A5489 | Other gonococcal infections |
A549 | Gonococcal infection, unspecified |
A811 | Subacute sclerosing panencephalitis |
A8182 | Gerstmann-Straussler-Scheinker syndrome |
A8183 | Fatal familial insomnia |
A8189 | Other atypical virus infections of central nervous system |
A830 | Japanese encephalitis |
A831 | Western equine encephalitis |
A832 | Eastern equine encephalitis |
A833 | St Louis encephalitis |
A834 | Australian encephalitis |
A835 | California encephalitis |
A836 | Rocio virus disease |
A838 | Other mosquito-borne viral encephalitis |
A839 | Mosquito-borne viral encephalitis, unspecified |
A840 | Far Eastern tick-borne encephalitis [Russian spring-summer encephalitis] |
A841 | Central European tick-borne encephalitis |
A8481 | Powassan virus disease |
A8489 | Other tick-borne viral encephalitis |
A849 | Tick-borne viral encephalitis, unspecified |
A850 | Enteroviral encephalitis |
A851 | Adenoviral encephalitis |
A852 | Arthropod-borne viral encephalitis, unspecified |
A858 | Other specified viral encephalitis |
A870 | Enteroviral meningitis |
A871 | Adenoviral meningitis |
A872 | Lymphocytic choriomeningitis |
A878 | Other viral meningitis |
A879 | Viral meningitis, unspecified |
A880 | Enteroviral exanthematous fever [Boston exanthem] |
A888 | Other specified viral infections of central nervous system |
A921 | O'nyong-nyong fever |
A922 | Venezuelan equine fever |
A9230 | West Nile virus infection, unspecified |
A9231 | West Nile virus infection with encephalitis |
A9232 | West Nile virus infection with other neurologic manifestation |
A9239 | West Nile virus infection with other complications |
A924 | Rift Valley fever |
A925 | Zika virus disease |
A928 | Other specified mosquito-borne viral fevers |
A930 | Oropouche virus disease |
A962 | Lassa fever |
A983 | Marburg virus disease |
A984 | Ebola virus disease |
B003 | Herpesviral meningitis |
B004 | Herpesviral encephalitis |
B0089 | Other herpesviral infection |
B009 | Herpesviral infection, unspecified |
B010 | Varicella meningitis |
B0111 | Varicella encephalitis and encephalomyelitis |
B0181 | Varicella keratitis |
B0189 | Other varicella complications |
B019 | Varicella without complication |
B020 | Zoster encephalitis |
B021 | Zoster meningitis |
B0221 | Postherpetic geniculate ganglionitis |
B0222 | Postherpetic trigeminal neuralgia |
B0223 | Postherpetic polyneuropathy |
B0229 | Other postherpetic nervous system involvement |
B027 | Disseminated zoster |
B028 | Zoster with other complications |
B029 | Zoster without complications |
B04 | Monkeypox |
B0601 | Rubella encephalitis |
B0804 | Paravaccinia, unspecified |
B0809 | Other orthopoxvirus infections |
B0820 | Exanthema subitum [sixth disease], unspecified |
B0821 | Exanthema subitum [sixth disease] due to human herpesvirus 6 |
B0822 | Exanthema subitum [sixth disease] due to human herpesvirus 7 |
B0860 | Parapoxvirus infection, unspecified |
B0861 | Bovine stomatitis |
B0862 | Sealpox |
B0869 | Other parapoxvirus infections |
B0870 | Yatapoxvirus infection, unspecified |
B0871 | Tanapox virus disease |
B0872 | Yaba pox virus disease |
B0879 | Other yatapoxvirus infections |
B09 | Unspecified viral infection characterized by skin and mucous membrane lesions |
B1001 | Human herpesvirus 6 encephalitis |
B1009 | Other human herpesvirus encephalitis |
B1081 | Human herpesvirus 6 infection |
B1082 | Human herpesvirus 7 infection |
B1089 | Other human herpesvirus infection |
B261 | Mumps meningitis |
B262 | Mumps encephalitis |
B2700 | Gammaherpesviral mononucleosis without complication |