PDX Collection 4373 (continued) |
D68311 | Acquired hemophilia |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7581 | Myelofibrosis |
D7582 | Heparin induced thrombocytopenia (HIT) |
D75838 | Other thrombocytosis |
D75839 | Thrombocytosis, unspecified |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 4374 |
D474 | Osteomyelofibrosis |
D65 | Disseminated intravascular coagulation [defibrination syndrome] |
D66 | Hereditary factor VIII deficiency |
D67 | Hereditary factor IX deficiency |
D680 | Von Willebrand's disease |
D681 | Hereditary factor XI deficiency |
D682 | Hereditary deficiency of other clotting factors |
D68311 | Acquired hemophilia |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7581 | Myelofibrosis |
D7582 | Heparin induced thrombocytopenia (HIT) |
D75838 | Other thrombocytosis |
D75839 | Thrombocytosis, unspecified |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 4375 |
D474 | Osteomyelofibrosis |
D65 | Disseminated intravascular coagulation [defibrination syndrome] |
D66 | Hereditary factor VIII deficiency |
D67 | Hereditary factor IX deficiency |
D680 | Von Willebrand's disease |
D681 | Hereditary factor XI deficiency |
D682 | Hereditary deficiency of other clotting factors |
D68311 | Acquired hemophilia |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D68318 | Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors |
D6832 | Hemorrhagic disorder due to extrinsic circulating anticoagulants |
D684 | Acquired coagulation factor deficiency |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D688 | Other specified coagulation defects |
D689 | Coagulation defect, unspecified |
D690 | Allergic purpura |
D691 | Qualitative platelet defects |
D692 | Other nonthrombocytopenic purpura |
D693 | Immune thrombocytopenic purpura |
D6941 | Evans syndrome |
D6942 | Congenital and hereditary thrombocytopenia purpura |
D6949 | Other primary thrombocytopenia |
D6951 | Posttransfusion purpura |
D6959 | Other secondary thrombocytopenia |
D696 | Thrombocytopenia, unspecified |
D698 | Other specified hemorrhagic conditions |
D699 | Hemorrhagic condition, unspecified |
D7581 | Myelofibrosis |
D7582 | Heparin induced thrombocytopenia (HIT) |
D75838 | Other thrombocytosis |
D75839 | Thrombocytosis, unspecified |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 4376 |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
E7040 | Disorders of histidine metabolism, unspecified |
E7041 | Histidinemia |
E7049 | Other disorders of histidine metabolism |
E705 | Disorders of tryptophan metabolism |
E7081 | Aromatic L-amino acid decarboxylase deficiency |
E7089 | Other disorders of aromatic amino-acid metabolism |
E709 | Disorder of aromatic amino-acid metabolism, unspecified |
E710 | Maple-syrup-urine disease |
E71110 | Isovaleric acidemia |
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 | 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 |
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 |
E75244 | Niemann-Pick disease type A/B |
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 |
E7841 | Elevated Lipoprotein(a) |
E7849 | 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 |
E8802 | Plasminogen deficiency |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
|
PDX Collection 4377 |
F070 | Personality change due to known physiological condition |
F0781 | Postconcussional syndrome |
F079 | Unspecified personality and behavioral disorder due to known physiological condition |
F09 | Unspecified mental disorder due to known physiological condition |
F200 | Paranoid schizophrenia |
F201 | Disorganized schizophrenia |
F202 | Catatonic schizophrenia |
F203 | Undifferentiated schizophrenia |
F205 | Residual schizophrenia |
F2081 | Schizophreniform disorder |
F2089 | Other schizophrenia |
F209 | Schizophrenia, unspecified |
F21 | Schizotypal disorder |
F22 | Delusional disorders |
F23 | Brief psychotic disorder |
F24 | Shared psychotic disorder |
F250 | Schizoaffective disorder, bipolar type |
F251 | Schizoaffective disorder, depressive type |
F258 | Other schizoaffective disorders |
F259 | Schizoaffective disorder, unspecified |
F28 | Other psychotic disorder not due to a substance or known physiological condition |
F29 | Unspecified psychosis not due to a substance or known physiological condition |
F3010 | Manic episode without psychotic symptoms, unspecified |
F3011 | Manic episode without psychotic symptoms, mild |
F3012 | Manic episode without psychotic symptoms, moderate |
F3013 | Manic episode, severe, without psychotic symptoms |
F302 | Manic episode, severe with psychotic symptoms |
F303 | Manic episode in partial remission |
F304 | Manic episode in full remission |
F308 | Other manic episodes |
F309 | Manic episode, unspecified |
F310 | Bipolar disorder, current episode hypomanic |
F3110 | Bipolar disorder, current episode manic without psychotic features, unspecified |
F3111 | Bipolar disorder, current episode manic without psychotic features, mild |
F3112 | Bipolar disorder, current episode manic without psychotic features, moderate |
F3113 | Bipolar disorder, current episode manic without psychotic features, severe |
F312 | Bipolar disorder, current episode manic severe with psychotic features |
F3130 | Bipolar disorder, current episode depressed, mild or moderate severity, unspecified |
F3131 | Bipolar disorder, current episode depressed, mild |
F3132 | Bipolar disorder, current episode depressed, moderate |
F314 | Bipolar disorder, current episode depressed, severe, without psychotic features |
F315 | Bipolar disorder, current episode depressed, severe, with psychotic features |
F3160 | Bipolar disorder, current episode mixed, unspecified |
F3161 | Bipolar disorder, current episode mixed, mild |
F3162 | Bipolar disorder, current episode mixed, moderate |
F3163 | Bipolar disorder, current episode mixed, severe, without psychotic features |
F3164 | Bipolar disorder, current episode mixed, severe, with psychotic features |
F3170 | Bipolar disorder, currently in remission, most recent episode unspecified |
F3171 | Bipolar disorder, in partial remission, most recent episode hypomanic |
F3172 | Bipolar disorder, in full remission, most recent episode hypomanic |
F3173 | Bipolar disorder, in partial remission, most recent episode manic |
F3174 | Bipolar disorder, in full remission, most recent episode manic |
F3175 | Bipolar disorder, in partial remission, most recent episode depressed |
F3176 | Bipolar disorder, in full remission, most recent episode depressed |
F3177 | Bipolar disorder, in partial remission, most recent episode mixed |
F3178 | Bipolar disorder, in full remission, most recent episode mixed |
F3181 | Bipolar II disorder |
F3189 | Other bipolar disorder |
F319 | Bipolar disorder, unspecified |
F320 | Major depressive disorder, single episode, mild |
F321 | Major depressive disorder, single episode, moderate |
F322 | Major depressive disorder, single episode, severe without psychotic features |
F323 | Major depressive disorder, single episode, severe with psychotic features |
F324 | Major depressive disorder, single episode, in partial remission |
F325 | Major depressive disorder, single episode, in full remission |
F3281 | Premenstrual dysphoric disorder |
F3289 | Other specified depressive episodes |
F329 | Major depressive disorder, single episode, unspecified |
F32A | Depression, unspecified |
F330 | Major depressive disorder, recurrent, mild |
F331 | Major depressive disorder, recurrent, moderate |
F332 | Major depressive disorder, recurrent severe without psychotic features |
F333 | Major depressive disorder, recurrent, severe with psychotic symptoms |
F3340 | Major depressive disorder, recurrent, in remission, unspecified |
F3341 | Major depressive disorder, recurrent, in partial remission |
F3342 | Major depressive disorder, recurrent, in full remission |
F338 | Other recurrent depressive disorders |
F339 | Major depressive disorder, recurrent, unspecified |
F340 | Cyclothymic disorder |
F341 | Dysthymic disorder |
F3481 | Disruptive mood dysregulation disorder |
F3489 | Other specified persistent mood disorders |
F349 | Persistent mood [affective] disorder, unspecified |
F39 | Unspecified mood [affective] disorder |
F4000 | Agoraphobia, unspecified |
F4001 | Agoraphobia with panic disorder |
F4002 | Agoraphobia without panic disorder |
F4010 | Social phobia, unspecified |
F4011 | Social phobia, generalized |
F40210 | Arachnophobia |
F40218 | Other animal type phobia |
F40220 | Fear of thunderstorms |
F40228 | Other natural environment type phobia |
F40230 | Fear of blood |
F40231 | Fear of injections and transfusions |
F40232 | Fear of other medical care |
F40233 | Fear of injury |
F40240 | Claustrophobia |
F40241 | Acrophobia |
F40242 | Fear of bridges |
F40243 | Fear of flying |
F40248 | Other situational type phobia |
F40290 | Androphobia |
F40291 | Gynephobia |
F40298 | Other specified phobia |
F408 | Other phobic anxiety disorders |
F409 | Phobic anxiety disorder, unspecified |
F410 | Panic disorder [episodic paroxysmal anxiety] |
F411 | Generalized anxiety disorder |
F413 | Other mixed anxiety disorders |
F418 | Other specified anxiety disorders |
F419 | Anxiety disorder, unspecified |
F422 | Mixed obsessional thoughts and acts |
F423 | Hoarding disorder |
F424 | Excoriation (skin-picking) disorder |
F428 | Other obsessive-compulsive disorder |
F429 | Obsessive-compulsive disorder, unspecified |
F430 | Acute stress reaction |
F4310 | Post-traumatic stress disorder, unspecified |
F4311 | Post-traumatic stress disorder, acute |
F4312 | Post-traumatic stress disorder, chronic |
F4320 | Adjustment disorder, unspecified |
F4321 | Adjustment disorder with depressed mood |
F4322 | Adjustment disorder with anxiety |
F4323 | Adjustment disorder with mixed anxiety and depressed mood |
F4324 | Adjustment disorder with disturbance of conduct |
F4325 | Adjustment disorder with mixed disturbance of emotions and conduct |
F4329 | Adjustment disorder with other symptoms |
F438 | Other reactions to severe stress |
F439 | Reaction to severe stress, unspecified |
F440 | Dissociative amnesia |
F441 | Dissociative fugue |
F442 | Dissociative stupor |
F444 | Conversion disorder with motor symptom or deficit |
F445 | Conversion disorder with seizures or convulsions |
F446 | Conversion disorder with sensory symptom or deficit |
F447 | Conversion disorder with mixed symptom presentation |
F4481 | Dissociative identity disorder |
F4489 | Other dissociative and conversion disorders |
F449 | Dissociative and conversion disorder, unspecified |
F450 | Somatization disorder |
F451 | Undifferentiated somatoform disorder |
F4520 | Hypochondriacal disorder, unspecified |
F4521 | Hypochondriasis |
F4522 | Body dysmorphic disorder |
F4529 | Other hypochondriacal disorders |
F4541 | Pain disorder exclusively related to psychological factors |
F4542 | Pain disorder with related psychological factors |
F458 | Other somatoform disorders |
F459 | Somatoform disorder, unspecified |
F481 | Depersonalization-derealization syndrome |
F488 | Other specified nonpsychotic mental disorders |
F489 | Nonpsychotic mental 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 |
F5101 | Primary insomnia |