Llc Condition
Llc Condition
Llc Condition
Obs ICD10
185 B20
258 B9735
1465 D561
1466 D562
1467 D565
1468 D5700
1469 D5701
1470 D5702
1471 D5703
1472 D5709
1473 D571
1474 D5742
1475 D57431
1476 D57432
1477 D57433
1478 D57438
1479 D57439
1514 D66
1516 D67
1573 D810
1574 D811
1575 D812
1576 D8130
1577 D8131
1578 D8132
1579 D8139
1580 D814
1581 D815
1582 D816
1583 D817
1584 D8182
1585 D8189
1586 D819
1587 D820
1588 D821
1595 D831
1600 D841
1618 D89810
1619 D89811
1620 D89812
1621 D89813
2123 E700
2124 E701
2125 E7020
2126 E7021
2127 E7029
2128 E7030
2129 E70310
2130 E70311
2131 E70318
2132 E70319
2133 E70320
2134 E70321
2135 E70328
2136 E70329
2137 E70330
2138 E70331
2139 E70338
2140 E70339
2141 E7039
2142 E7040
2143 E7041
2144 E7049
2145 E705
2146 E7081
2147 E7089
2148 E709
2149 E710
2150 E71110
2151 E71111
2152 E71118
2153 E71120
2154 E71121
2155 E71128
2156 E7119
2157 E712
2158 E7130
2159 E71310
2160 E71311
2161 E71312
2162 E71313
2163 E71314
2164 E71318
2165 E7132
2166 E7139
2167 E7140
2168 E7141
2169 E7142
2170 E7143
2171 E71440
2172 E71448
2173 E7150
2174 E71510
2175 E71511
2176 E71518
2177 E71520
2178 E71521
2179 E71522
2180 E71528
2181 E71529
2182 E7153
2183 E71540
2184 E71541
2185 E71542
2186 E71548
2187 E7200
2188 E7201
2189 E7202
2190 E7203
2191 E7204
2192 E7209
2193 E7210
2194 E7211
2195 E7212
2196 E7219
2197 E7220
2198 E7221
2199 E7222
2200 E7223
2201 E7229
2202 E723
2203 E724
2204 E7250
2205 E7251
2206 E7252
2207 E7253
2208 E7259
2209 E7281
2210 E7289
2211 E729
2212 E7400
2213 E7401
2214 E7402
2215 E7403
2216 E7404
2217 E7409
2218 E7420
2219 E7421
2220 E7429
2221 E744
2222 E74810
2223 E74818
2224 E74819
2225 E7489
2226 E749
2227 E7500
2228 E7501
2229 E7502
2230 E7509
2231 E7510
2232 E7511
2233 E7519
2234 E7521
2235 E7522
2236 E7523
2237 E75240
2238 E75241
2239 E75242
2240 E75243
2241 E75244
2242 E75248
2243 E75249
2244 E7525
2245 E7526
2246 E7529
2247 E753
2248 E754
2249 E7601
2250 E7602
2251 E7603
2252 E761
2253 E76210
2254 E76211
2255 E76219
2256 E7622
2257 E7629
2258 E763
2259 E768
2260 E769
2261 E770
2262 E771
2263 E778
2264 E779
2265 E7871
2266 E7872
2267 E791
2268 E792
2269 E798
2270 E799
2271 E800
2272 E801
2273 E8020
2274 E8021
2275 E8029
2276 E803
2277 E8300
2278 E8301
2279 E8309
2280 E840
2281 E8411
2282 E8419
2283 E848
2284 E849
2285 E850
2286 E851
2287 E852
2288 E853
2289 E854
2290 E8581
2291 E8582
2292 E8589
2293 E859
2294 E8801
2296 E8840
2297 E8841
2298 E8842
2299 E8849
2300 E8889
2778 F840
2779 F842
2780 F843
2781 F845
2782 F848
2783 F849
2818 G10
2819 G110
2820 G1110
2821 G1111
2822 G1119
2823 G112
2824 G113
2825 G114
2826 G118
2827 G119
2828 G120
2829 G121
2830 G1220
2831 G1221
2832 G1222
2833 G1223
2834 G1224
2835 G1225
2836 G1229
2837 G128
2838 G129
2841 G20
2842 G2111
2843 G2119
2844 G212
2845 G213
2846 G214
2847 G218
2848 G219
2849 G230
2850 G231
2851 G232
2852 G238
2853 G239
2854 G3181
2855 G3182
2857 G3281
2858 G35
2859 G360
2860 G370
2863 G375
2914 G47411
2915 G47419
2916 G47421
2917 G47429
2918 G546
2919 G547
2943 G7100
2944 G7101
2945 G7102
2946 G71031
2947 G71032
2948 G71033
2949 G710340
2950 G710341
2951 G710342
2952 G710349
2953 G71035
2954 G71038
2955 G71039
2956 G7109
2957 G7111
2958 G7120
2959 G7121
2960 G71220
2961 G71228
2962 G7129
2965 G800
2966 G801
2967 G802
2968 G803
2969 G804
2970 G808
2971 G809
2987 G8220
2988 G8221
2989 G8222
2990 G8250
2991 G8251
2992 G8252
2993 G8253
2994 G8254
3019 G901
3020 G903
3031 G937
3041 H353210
3042 H353211
3043 H353212
3044 H353213
3045 H353220
3046 H353221
3047 H353222
3048 H353223
3049 H353230
3050 H353231
3051 H353232
3052 H353233
3053 H353290
3054 H353291
3055 H353292
3056 H353293
3057 H49811
3058 H49812
3059 H49813
3060 H49819
3836 I8500
3837 I8501
3838 I8510
3839 I8511
4179 K7040
4180 K7041
4190 K7210
4191 K7211
4192 K7290
4193 K7291
4209 K766
4210 K767
4211 K7681
4212 K7682
5149 M3111
8361 P570
8362 P578
8363 P579
8400 Q000
8401 Q001
8402 Q002
8403 Q010
8404 Q011
8405 Q012
8406 Q018
8407 Q019
8408 Q02
8413 Q040
8414 Q041
8415 Q042
8416 Q043
8417 Q044
8418 Q045
8419 Q046
8420 Q048
8421 Q049
8422 Q050
8423 Q051
8424 Q052
8425 Q053
8426 Q054
8427 Q055
8428 Q056
8429 Q057
8430 Q058
8431 Q059
8432 Q060
8433 Q061
8434 Q062
8435 Q063
8436 Q064
8437 Q068
8438 Q069
8439 Q0700
8440 Q0701
8441 Q0702
8442 Q0703
8443 Q078
8444 Q079
8607 Q773
8610 Q776
8614 Q780
8615 Q781
8616 Q782
8617 Q783
8619 Q785
8620 Q786
8621 Q788
8622 Q789
8651 Q860
8652 Q861
8653 Q862
8654 Q868
8655 Q8711
8656 Q8719
8657 Q872
8658 Q873
8664 Q875
8665 Q8781
8667 Q8789
8669 Q894
8671 Q898
8672 Q900
8673 Q901
8674 Q902
8675 Q909
8676 Q910
8677 Q911
8678 Q912
8679 Q913
8680 Q914
8681 Q915
8682 Q916
8683 Q917
8684 Q920
8685 Q921
8686 Q922
8687 Q925
8688 Q9261
8689 Q9262
8690 Q927
8691 Q928
8692 Q929
8693 Q930
8694 Q931
8695 Q932
8696 Q933
8697 Q934
8698 Q9351
8699 Q9359
8700 Q937
8701 Q9381
8702 Q9382
8703 Q9388
8704 Q9389
8705 Q939
8706 Q952
8707 Q953
8708 Q960
8709 Q961
8710 Q962
8711 Q963
8712 Q964
8713 Q968
8714 Q969
8715 Q970
8716 Q971
8717 Q972
8718 Q973
8719 Q978
8720 Q979
8721 Q980
8722 Q981
8723 Q983
8724 Q984
8725 Q985
8726 Q986
8727 Q987
8728 Q988
8729 Q989
8730 Q990
8731 Q991
8732 Q992
8733 Q998
8734 Q999
8779 R532
9040 S14111D
9041 S14111S
9043 S14112D
9044 S14112S
9046 S14113D
9047 S14113S
9049 S14114D
9050 S14114S
9052 S14115D
9053 S14115S
9055 S14116D
9056 S14116S
9058 S14117D
9059 S14117S
9061 S14118D
9062 S14118S
9064 S14119D
9065 S14119S
9283 S24111D
9284 S24111S
9286 S24112D
9287 S24112S
9289 S24113D
9290 S24113S
9292 S24114D
9293 S24114S
9295 S24119D
9296 S24119S
10804 T8600
10805 T8601
10806 T8602
10807 T8603
10808 T8609
10809 T8610
10810 T8611
10811 T8612
10812 T8613
10813 T8619
10814 T8620
10815 T8621
10816 T8622
10817 T8623
10818 T86290
10819 T86298
10820 T8630
10821 T8631
10822 T8632
10823 T8633
10824 T8639
10825 T8640
10826 T8641
10827 T8642
10828 T8643
10829 T8649
10830 T865
10831 T86810
10832 T86811
10833 T86812
10834 T86818
10835 T86819
10836 T86850
10837 T86851
10838 T86852
10839 T86858
10840 T86859
10908 Z21
11027 Z44001
11028 Z44002
11029 Z44009
11030 Z44011
11031 Z44012
11032 Z44019
11033 Z44021
11034 Z44022
11035 Z44029
11036 Z44101
11037 Z44102
11038 Z44109
11039 Z44111
11040 Z44112
11041 Z44119
11042 Z44121
11043 Z44122
11044 Z44129
11045 Z4821
11046 Z4822
11047 Z4823
11048 Z4824
11049 Z48280
11050 Z48290
11052 Z89111
11053 Z89112
11054 Z89119
11055 Z89121
11056 Z89122
11057 Z89129
11058 Z89201
11059 Z89202
11060 Z89209
11061 Z89211
11062 Z89212
11063 Z89219
11064 Z89221
11065 Z89222
11066 Z89229
11067 Z89431
11068 Z89432
11069 Z89439
11070 Z89441
11071 Z89442
11072 Z89449
11073 Z89511
11074 Z89512
11075 Z89519
11076 Z89611
11077 Z89612
11078 Z89619
11079 Z899
11092 Z940
11093 Z941
11094 Z942
11095 Z943
11096 Z944
11097 Z9481
11098 Z9482
11099 Z9483
11100 Z9484
11103 Z9710
11104 Z9711
11105 Z9712
11106 Z9713
11107 Z9714
11108 Z9715
11109 Z9716
Notes:
1. ICD-10 code O021: A missed abortion is a type of miscarriage (also referred to as a delayed miscarriage).
2. ICD-10 codes O03 and O311 ranges: A spontaneous abortion is spontaneous loss of the fetus before the 20th week of pregn
3. ICD-10 code O200: A threatened abortion refers to a hemorrhage in early pregnancy (also referred to as a threatened misca
Output: diy_icd10_udxgv0123_hccv07.modelICD10list.table3.xlsx
Source: RTI International
CD-10 to V07 HHS-Condition Categories (CC) Crosswalk
iscal Year (FY) 2022 and FY2023 list of ICD-10 codes.
ICD10 Label
Human immunodeficiency virus [HIV] disease
Human immunodeficiency virus, type 2 [HIV 2] as the cause of diseases classified elsewhere
Beta thalassemia
Delta-beta thalassemia
Hemoglobin E-beta thalassemia
Hb-SS disease with crisis, unspecified
Hb-SS disease with acute chest syndrome
Hb-SS disease with splenic sequestration
Hb-SS disease with cerebral vascular involvement
Hb-SS disease with crisis with other specified complication
Sickle-cell disease without crisis
Sickle-cell thalassemia beta zero without crisis
Sickle-cell thalassemia beta zero with acute chest syndrome
Sickle-cell thalassemia beta zero with splenic sequestration
Sickle-cell thalassemia beta zero with cerebral vascular involvement
Sickle-cell thalassemia beta zero with crisis with other specified complication
Sickle-cell thalassemia beta zero with crisis, unspecified
Hereditary factor VIII deficiency
Hereditary factor IX deficiency
Severe combined immunodeficiency [SCID] with reticular dysgenesis
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
Adenosine deaminase deficiency, unspecified
Severe combined immunodeficiency due to adenosine deaminase deficiency
Adenosine deaminase 2 deficiency
Other adenosine deaminase deficiency
Nezelof's syndrome
Purine nucleoside phosphorylase [PNP] deficiency
Major histocompatibility complex class I deficiency
Major histocompatibility complex class II deficiency
Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
Other combined immunodeficiencies
Combined immunodeficiency, unspecified
Wiskott-Aldrich syndrome
Di George's syndrome
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
Defects in the complement system
Acute graft-versus-host disease
Chronic graft-versus-host disease
Acute on chronic graft-versus-host disease
Graft-versus-host disease, unspecified
Classical phenylketonuria
Other hyperphenylalaninemias
Disorder of tyrosine metabolism, unspecified
Tyrosinemia
Other disorders of tyrosine metabolism
Albinism, unspecified
X-linked ocular albinism
Autosomal recessive ocular albinism
Other ocular albinism
Ocular albinism, unspecified
Tyrosinase negative oculocutaneous albinism
Tyrosinase positive oculocutaneous albinism
Other oculocutaneous albinism
Oculocutaneous albinism, unspecified
Chediak-Higashi syndrome
Hermansky-Pudlak syndrome
Other albinism with hematologic abnormality
Albinism with hematologic abnormality, unspecified
Other specified albinism
Disorders of histidine metabolism, unspecified
Histidinemia
Other disorders of histidine metabolism
Disorders of tryptophan metabolism
Aromatic L-amino acid decarboxylase deficiency
Other disorders of aromatic amino-acid metabolism
Disorder of aromatic amino-acid metabolism, unspecified
Maple-syrup-urine disease
Isovaleric acidemia
3-methylglutaconic aciduria
Other branched-chain organic acidurias
Methylmalonic acidemia
Propionic acidemia
Other disorders of propionate metabolism
Other disorders of branched-chain amino-acid metabolism
Disorder of branched-chain amino-acid metabolism, unspecified
Disorder of fatty-acid metabolism, unspecified
Long chain/very long chain acyl CoA dehydrogenase deficiency
Medium chain acyl CoA dehydrogenase deficiency
Short chain acyl CoA dehydrogenase deficiency
Glutaric aciduria type II
Muscle carnitine palmitoyltransferase deficiency
Other disorders of fatty-acid oxidation
Disorders of ketone metabolism
Other disorders of fatty-acid metabolism
Disorder of carnitine metabolism, unspecified
Primary carnitine deficiency
Carnitine deficiency due to inborn errors of metabolism
Iatrogenic carnitine deficiency
Ruvalcaba-Myhre-Smith syndrome
Other secondary carnitine deficiency
Peroxisomal disorder, unspecified
Zellweger syndrome
Neonatal adrenoleukodystrophy
Other disorders of peroxisome biogenesis
Childhood cerebral X-linked adrenoleukodystrophy
Adolescent X-linked adrenoleukodystrophy
Adrenomyeloneuropathy
Other X-linked adrenoleukodystrophy
X-linked adrenoleukodystrophy, unspecified type
Other group 2 peroxisomal disorders
Rhizomelic chondrodysplasia punctata
Zellweger-like syndrome
Other group 3 peroxisomal disorders
Other peroxisomal disorders
Disorders of amino-acid transport, unspecified
Cystinuria
Hartnup's disease
Lowe's syndrome
Cystinosis
Other disorders of amino-acid transport
Disorders of sulfur-bearing amino-acid metabolism, unspecified
Homocystinuria
Methylenetetrahydrofolate reductase deficiency
Other disorders of sulfur-bearing amino-acid metabolism
Disorder of urea cycle metabolism, unspecified
Argininemia
Arginosuccinic aciduria
Citrullinemia
Other disorders of urea cycle metabolism
Disorders of lysine and hydroxylysine metabolism
Disorders of ornithine metabolism
Disorder of glycine metabolism, unspecified
Non-ketotic hyperglycinemia
Trimethylaminuria
Primary hyperoxaluria
Other disorders of glycine metabolism
Disorders of gamma aminobutyric acid metabolism
Other specified disorders of amino-acid metabolism
Disorder of amino-acid metabolism, unspecified
Glycogen storage disease, unspecified
von Gierke disease
Pompe disease
Cori disease
McArdle disease
Other glycogen storage disease
Disorders of galactose metabolism, unspecified
Galactosemia
Other disorders of galactose metabolism
Disorders of pyruvate metabolism and gluconeogenesis
Glucose transporter protein type 1 deficiency
Other disorders of glucose transport
Disorders of glucose transport, unspecified
Other specified disorders of carbohydrate metabolism
Disorder of carbohydrate metabolism, unspecified
GM2 gangliosidosis, unspecified
Sandhoff disease
Tay-Sachs disease
Other GM2 gangliosidosis
Unspecified gangliosidosis
Mucolipidosis IV
Other gangliosidosis
Fabry (-Anderson) disease
Gaucher disease
Krabbe disease
Niemann-Pick disease type A
Niemann-Pick disease type B
Niemann-Pick disease type C
Niemann-Pick disease type D
Niemann-Pick disease type A/B
Other Niemann-Pick disease
Niemann-Pick disease, unspecified
Metachromatic leukodystrophy
Sulfatase deficiency
Other sphingolipidosis
Sphingolipidosis, unspecified
Neuronal ceroid lipofuscinosis
Hurler's syndrome
Hurler-Scheie syndrome
Scheie's syndrome
Mucopolysaccharidosis, type II
Morquio A mucopolysaccharidoses
Morquio B mucopolysaccharidoses
Morquio mucopolysaccharidoses, unspecified
Sanfilippo mucopolysaccharidoses
Other mucopolysaccharidoses
Mucopolysaccharidosis, unspecified
Other disorders of glucosaminoglycan metabolism
Glucosaminoglycan metabolism disorder, unspecified
Defects in post-translational modification of lysosomal enzymes
Defects in glycoprotein degradation
Other disorders of glycoprotein metabolism
Disorder of glycoprotein metabolism, unspecified
Barth syndrome
Smith-Lemli-Opitz syndrome
Lesch-Nyhan syndrome
Myoadenylate deaminase deficiency
Other disorders of purine and pyrimidine metabolism
Disorder of purine and pyrimidine metabolism, unspecified
Hereditary erythropoietic porphyria
Porphyria cutanea tarda
Unspecified porphyria
Acute intermittent (hepatic) porphyria
Other porphyria
Defects of catalase and peroxidase
Disorder of copper metabolism, unspecified
Wilson's disease
Other disorders of copper metabolism
Cystic fibrosis with pulmonary manifestations
Meconium ileus in cystic fibrosis
Cystic fibrosis with other intestinal manifestations
Cystic fibrosis with other manifestations
Cystic fibrosis, unspecified
Non-neuropathic heredofamilial amyloidosis
Neuropathic heredofamilial amyloidosis
Heredofamilial amyloidosis, unspecified
Secondary systemic amyloidosis
Organ-limited amyloidosis
Light chain (AL) amyloidosis
Wild-type transthyretin-related (ATTR) amyloidosis
Other amyloidosis
Amyloidosis, unspecified
Alpha-1-antitrypsin deficiency
Mitochondrial metabolism disorder, unspecified
MELAS syndrome
MERRF syndrome
Other mitochondrial metabolism disorders
Other specified metabolic disorders
Autistic disorder
Rett's syndrome
Other childhood disintegrative disorder
Asperger's syndrome
Other pervasive developmental disorders
Pervasive developmental disorder, unspecified
Huntington's disease
Congenital nonprogressive ataxia
Early-onset cerebellar ataxia, unspecified
Friedreich ataxia
Other early-onset cerebellar ataxia
Late-onset cerebellar ataxia
Cerebellar ataxia with defective DNA repair
Hereditary spastic paraplegia
Other hereditary ataxias
Hereditary ataxia, unspecified
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
Other inherited spinal muscular atrophy
Motor neuron disease, unspecified
Amyotrophic lateral sclerosis
Progressive bulbar palsy
Primary lateral sclerosis
Familial motor neuron disease
Progressive spinal muscle atrophy
Other motor neuron disease
Other spinal muscular atrophies and related syndromes
Spinal muscular atrophy, unspecified
Parkinson's disease
Neuroleptic induced parkinsonism
Other drug induced secondary parkinsonism
Secondary parkinsonism due to other external agents
Postencephalitic parkinsonism
Vascular parkinsonism
Other secondary parkinsonism
Secondary parkinsonism, unspecified
Hallervorden-Spatz disease
Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
Striatonigral degeneration
Other specified degenerative diseases of basal ganglia
Degenerative disease of basal ganglia, unspecified
Alpers disease
Leigh's disease
Cerebellar ataxia in diseases classified elsewhere
Multiple sclerosis
Neuromyelitis optica [Devic]
Diffuse sclerosis of central nervous system
Concentric sclerosis [Balo] of central nervous system
Narcolepsy with cataplexy
Narcolepsy without cataplexy
Narcolepsy in conditions classified elsewhere with cataplexy
Narcolepsy in conditions classified elsewhere without cataplexy
Phantom limb syndrome with pain
Phantom limb syndrome without pain
Muscular dystrophy, unspecified
Duchenne or Becker muscular dystrophy
Facioscapulohumeral muscular dystrophy
Autosomal dominant limb girdle muscular dystrophy
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Limb girdle muscular dystrophy due to dysferlin dysfunction
Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
Other limb girdle muscular dystrophy
Limb girdle muscular dystrophy, unspecified
Other specified muscular dystrophies
Myotonic muscular dystrophy
Congenital myopathy, unspecified
Nemaline myopathy
X-linked myotubular myopathy
Other centronuclear myopathy
Other congenital myopathy
Spastic quadriplegic cerebral palsy
Spastic diplegic cerebral palsy
Spastic hemiplegic cerebral palsy
Athetoid cerebral palsy
Ataxic cerebral palsy
Other cerebral palsy
Cerebral palsy, unspecified
Paraplegia, unspecified
Paraplegia, complete
Paraplegia, incomplete
Quadriplegia, unspecified
Quadriplegia, C1-C4 complete
Quadriplegia, C1-C4 incomplete
Quadriplegia, C5-C7 complete
Quadriplegia, C5-C7 incomplete
Familial dysautonomia [Riley-Day]
Multi-system degeneration of the autonomic nervous system
Reye's syndrome
Exudative age-related macular degeneration, right eye, stage unspecified
Exudative age-related macular degeneration, right eye, with active choroidal neovascularization
Exudative age-related macular degeneration, right eye, with inactive choroidal neovascularization
Exudative age-related macular degeneration, right eye, with inactive scar
Exudative age-related macular degeneration, left eye, stage unspecified
Exudative age-related macular degeneration, left eye, with active choroidal neovascularization
Exudative age-related macular degeneration, left eye, with inactive choroidal neovascularization
Exudative age-related macular degeneration, left eye, with inactive scar
Exudative age-related macular degeneration, bilateral, stage unspecified
Exudative age-related macular degeneration, bilateral, with active choroidal neovascularization
Exudative age-related macular degeneration, bilateral, with inactive choroidal neovascularization
Exudative age-related macular degeneration, bilateral, with inactive scar
Exudative age-related macular degeneration, unspecified eye, stage unspecified
Exudative age-related macular degeneration, unspecified eye, with active choroidal neovascularization
Exudative age-related macular degeneration, unspecified eye, with inactive choroidal neovascularization
Exudative age-related macular degeneration, unspecified eye, with inactive scar
Kearns-Sayre syndrome, right eye
Kearns-Sayre syndrome, left eye
Kearns-Sayre syndrome, bilateral
Kearns-Sayre syndrome, unspecified eye
Esophageal varices without bleeding
Esophageal varices with bleeding
Secondary esophageal varices without bleeding
Secondary esophageal varices with bleeding
Alcoholic hepatic failure without coma
Alcoholic hepatic failure with coma
Chronic hepatic failure without coma
Chronic hepatic failure with coma
Hepatic failure, unspecified without coma
Hepatic failure, unspecified with coma
Portal hypertension
Hepatorenal syndrome
Hepatopulmonary syndrome
Hepatic encephalopathy
Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA]
Kernicterus due to isoimmunization
Other specified kernicterus
Kernicterus, unspecified
Anencephaly
Craniorachischisis
Iniencephaly
Frontal encephalocele
Nasofrontal encephalocele
Occipital encephalocele
Encephalocele of other sites
Encephalocele, unspecified
Microcephaly
Congenital malformations of corpus callosum
Arhinencephaly
Holoprosencephaly
Other reduction deformities of brain
Septo-optic dysplasia of brain
Megalencephaly
Congenital cerebral cysts
Other specified congenital malformations of brain
Congenital malformation of brain, unspecified
Cervical spina bifida with hydrocephalus
Thoracic spina bifida with hydrocephalus
Lumbar spina bifida with hydrocephalus
Sacral spina bifida with hydrocephalus
Unspecified spina bifida with hydrocephalus
Cervical spina bifida without hydrocephalus
Thoracic spina bifida without hydrocephalus
Lumbar spina bifida without hydrocephalus
Sacral spina bifida without hydrocephalus
Spina bifida, unspecified
Amyelia
Hypoplasia and dysplasia of spinal cord
Diastematomyelia
Other congenital cauda equina malformations
Hydromyelia
Other specified congenital malformations of spinal cord
Congenital malformation of spinal cord, unspecified
Arnold-Chiari syndrome without spina bifida or hydrocephalus
Arnold-Chiari syndrome with spina bifida
Arnold-Chiari syndrome with hydrocephalus
Arnold-Chiari syndrome with spina bifida and hydrocephalus
Other specified congenital malformations of nervous system
Congenital malformation of nervous system, unspecified
Chondrodysplasia punctata
Chondroectodermal dysplasia
Osteogenesis imperfecta
Polyostotic fibrous dysplasia
Osteopetrosis
Progressive diaphyseal dysplasia
Metaphyseal dysplasia
Multiple congenital exostoses
Other specified osteochondrodysplasias
Osteochondrodysplasia, unspecified
Fetal alcohol syndrome (dysmorphic)
Fetal hydantoin syndrome
Dysmorphism due to warfarin
Other congenital malformation syndromes due to known exogenous causes
Prader-Willi syndrome
Other congenital malformation syndromes predominantly associated with short stature
Congenital malformation syndromes predominantly involving limbs
Congenital malformation syndromes involving early overgrowth
Other congenital malformation syndromes with other skeletal changes
Alport syndrome
Other specified congenital malformation syndromes, not elsewhere classified
Conjoined twins
Other specified congenital malformations
Trisomy 21, nonmosaicism (meiotic nondisjunction)
Trisomy 21, mosaicism (mitotic nondisjunction)
Trisomy 21, translocation
Down syndrome, unspecified
Trisomy 18, nonmosaicism (meiotic nondisjunction)
Trisomy 18, mosaicism (mitotic nondisjunction)
Trisomy 18, translocation
Trisomy 18, unspecified
Trisomy 13, nonmosaicism (meiotic nondisjunction)
Trisomy 13, mosaicism (mitotic nondisjunction)
Trisomy 13, translocation
Trisomy 13, unspecified
Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Partial trisomy
Duplications with other complex rearrangements
Marker chromosomes in normal individual
Marker chromosomes in abnormal individual
Triploidy and polyploidy
Other specified trisomies and partial trisomies of autosomes
Trisomy and partial trisomy of autosomes, unspecified
Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Chromosome replaced with ring, dicentric or isochromosome
Deletion of short arm of chromosome 4
Deletion of short arm of chromosome 5
Angelman syndrome
Other deletions of part of a chromosome
Deletions with other complex rearrangements
Velo-cardio-facial syndrome
Williams syndrome
Other microdeletions
Other deletions from the autosomes
Deletion from autosomes, unspecified
Balanced autosomal rearrangement in abnormal individual
Balanced sex/autosomal rearrangement in abnormal individual
Karyotype 45, X
Karyotype 46, X iso (Xq)
Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Mosaicism, 45, X/46, XX or XY
Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Other variants of Turner's syndrome
Turner's syndrome, unspecified
Karyotype 47, XXX
Female with more than three X chromosomes
Mosaicism, lines with various numbers of X chromosomes
Female with 46, XY karyotype
Other specified sex chromosome abnormalities, female phenotype
Sex chromosome abnormality, female phenotype, unspecified
Klinefelter syndrome karyotype 47, XXY
Klinefelter syndrome, male with more than two X chromosomes
Other male with 46, XX karyotype
Klinefelter syndrome, unspecified
Karyotype 47, XYY
Male with structurally abnormal sex chromosome
Male with sex chromosome mosaicism
Other specified sex chromosome abnormalities, male phenotype
Sex chromosome abnormality, male phenotype, unspecified
Chimera 46, XX/46, XY
46, XX true hermaphrodite
Fragile X chromosome
Other specified chromosome abnormalities
Chromosomal abnormality, unspecified
Functional quadriplegia
Complete lesion at C1 level of cervical spinal cord, subsequent encounter
Complete lesion at C1 level of cervical spinal cord, sequela
Complete lesion at C2 level of cervical spinal cord, subsequent encounter
Complete lesion at C2 level of cervical spinal cord, sequela
Complete lesion at C3 level of cervical spinal cord, subsequent encounter
Complete lesion at C3 level of cervical spinal cord, sequela
Complete lesion at C4 level of cervical spinal cord, subsequent encounter
Complete lesion at C4 level of cervical spinal cord, sequela
Complete lesion at C5 level of cervical spinal cord, subsequent encounter
Complete lesion at C5 level of cervical spinal cord, sequela
Complete lesion at C6 level of cervical spinal cord, subsequent encounter
Complete lesion at C6 level of cervical spinal cord, sequela
Complete lesion at C7 level of cervical spinal cord, subsequent encounter
Complete lesion at C7 level of cervical spinal cord, sequela
Complete lesion at C8 level of cervical spinal cord, subsequent encounter
Complete lesion at C8 level of cervical spinal cord, sequela
Complete lesion at unspecified level of cervical spinal cord, subsequent encounter
Complete lesion at unspecified level of cervical spinal cord, sequela
Complete lesion at T1 level of thoracic spinal cord, subsequent encounter
Complete lesion at T1 level of thoracic spinal cord, sequela
Complete lesion at T2-T6 level of thoracic spinal cord, subsequent encounter
Complete lesion at T2-T6 level of thoracic spinal cord, sequela
Complete lesion at T7-T10 level of thoracic spinal cord, subsequent encounter
Complete lesion at T7-T10 level of thoracic spinal cord, sequela
Complete lesion at T11-T12 level of thoracic spinal cord, subsequent encounter
Complete lesion at T11-T12 level of thoracic spinal cord, sequela
Complete lesion at unspecified level of thoracic spinal cord, subsequent encounter
Complete lesion at unspecified level of thoracic spinal cord, sequela
Unspecified complication of bone marrow transplant
Bone marrow transplant rejection
Bone marrow transplant failure
Bone marrow transplant infection
Other complications of bone marrow transplant
Unspecified complication of kidney transplant
Kidney transplant rejection
Kidney transplant failure
Kidney transplant infection
Other complication of kidney transplant
Unspecified complication of heart transplant
Heart transplant rejection
Heart transplant failure
Heart transplant infection
Cardiac allograft vasculopathy
Other complications of heart transplant
Unspecified complication of heart-lung transplant
Heart-lung transplant rejection
Heart-lung transplant failure
Heart-lung transplant infection
Other complications of heart-lung transplant
Unspecified complication of liver transplant
Liver transplant rejection
Liver transplant failure
Liver transplant infection
Other complications of liver transplant
Complications of stem cell transplant
Lung transplant rejection
Lung transplant failure
Lung transplant infection
Other complications of lung transplant
Unspecified complication of lung transplant
Intestine transplant rejection
Intestine transplant failure
Intestine transplant infection
Other complications of intestine transplant
Unspecified complication of intestine transplant
Asymptomatic human immunodeficiency virus [HIV] infection status
Encounter for fitting and adjustment of unspecified right artificial arm
Encounter for fitting and adjustment of unspecified left artificial arm
Encounter for fitting and adjustment of unspecified artificial arm, unspecified arm
Encounter for fitting and adjustment of complete right artificial arm
Encounter for fitting and adjustment of complete left artificial arm
Encounter for fitting and adjustment of complete artificial arm, unspecified arm
Encounter for fitting and adjustment of partial artificial right arm
Encounter for fitting and adjustment of partial artificial left arm
Encounter for fitting and adjustment of partial artificial arm, unspecified arm
Encounter for fitting and adjustment of unspecified right artificial leg
Encounter for fitting and adjustment of unspecified left artificial leg
Encounter for fitting and adjustment of unspecified artificial leg, unspecified leg
Encounter for fitting and adjustment of complete right artificial leg
Encounter for fitting and adjustment of complete left artificial leg
Encounter for fitting and adjustment of complete artificial leg, unspecified leg
Encounter for fitting and adjustment of partial artificial right leg
Encounter for fitting and adjustment of partial artificial left leg
Encounter for fitting and adjustment of partial artificial leg, unspecified leg
Encounter for aftercare following heart transplant
Encounter for aftercare following kidney transplant
Encounter for aftercare following liver transplant
Encounter for aftercare following lung transplant
Encounter for aftercare following heart-lung transplant
Encounter for aftercare following bone marrow transplant
Acquired absence of right hand
Acquired absence of left hand
Acquired absence of unspecified hand
Acquired absence of right wrist
Acquired absence of left wrist
Acquired absence of unspecified wrist
Acquired absence of right upper limb, unspecified level
Acquired absence of left upper limb, unspecified level
Acquired absence of unspecified upper limb, unspecified level
Acquired absence of right upper limb below elbow
Acquired absence of left upper limb below elbow
Acquired absence of unspecified upper limb below elbow
Acquired absence of right upper limb above elbow
Acquired absence of left upper limb above elbow
Acquired absence of unspecified upper limb above elbow
Acquired absence of right foot
Acquired absence of left foot
Acquired absence of unspecified foot
Acquired absence of right ankle
Acquired absence of left ankle
Acquired absence of unspecified ankle
Acquired absence of right leg below knee
Acquired absence of left leg below knee
Acquired absence of unspecified leg below knee
Acquired absence of right leg above knee
Acquired absence of left leg above knee
Acquired absence of unspecified leg above knee
Acquired absence of limb, unspecified
Kidney transplant status
Heart transplant status
Lung transplant status
Heart and lungs transplant status
Liver transplant status
Bone marrow transplant status
Intestine transplant status
Pancreas transplant status
Stem cells transplant status
Presence of artificial limb (complete) (partial), unspecified
Presence of artificial right arm (complete) (partial)
Presence of artificial left arm (complete) (partial)
Presence of artificial right leg (complete) (partial)
Presence of artificial left leg (complete) (partial)
Presence of artificial arms, bilateral (complete) (partial)
Presence of artificial legs, bilateral (complete) (partial)
code O021: A missed abortion is a type of miscarriage (also referred to as a delayed miscarriage).
codes O03 and O311 ranges: A spontaneous abortion is spontaneous loss of the fetus before the 20th week of pregnancy; also referred to
code O200: A threatened abortion refers to a hemorrhage in early pregnancy (also referred to as a threatened miscarriage).
iy_icd10_udxgv0123_hccv07.modelICD10list.table3.xlsx
TI International
CY2022 (FY22/FY23) MCE Age Condition [use AGE_AT
e ValidCode
in FY2022
FY2022
Valid (10/1/21
inMCE
FY2023
Age- (10/1/22
Condition
9/30/22)
FY2023
FY2022
- [use
9/30/23)
MCE MCE
AGE_AT_DIAGNOSIS]
AgeSex
Condition
Condition
FY2023
[use MCE _DIAGNOSIS]
AGE_AT_DIAGNOSIS]
Sex
CY2022
Condition
(FY22/FY23)
CC Age
MCE
Split
Sex[use
Condition
AGE_LAST]
CC Sex Split
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y male
Y Y male
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
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Y Y
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Y Y age = 0 age = 0 age = 0
Y Y
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Y Y
Y Y
Y Y
Y Y
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Y Y
Y Y
Y Y
Y Y
Y Y
Y Y 0 <= age <= 17 0 <= age <= 17 0 <= age <= 17
Y Y
Y Y
Y Y
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Y Y
Y Y
Y Y
Y Y
Y Y age >=15 age >=15 age >=15
Y Y
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Y Y 0 <= age <= 17 0 <= age <= 17 0 <= age <= 17
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y age >=15 age >=15 age >=15
Y Y
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Y Y
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N Y
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Y Y
Y Y
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Y Y
Y Y
Y Y
Y Y
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y female female female
Y Y male male male
Y Y male male male
Y Y male male male
Y Y male male male
Y Y
Y Y male male male
Y Y male male male
Y Y male male male
Y Y male male male
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
Y Y
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