ICD10_Master_list

Modification Stamp: 2023-07-25T07:00:00	1
A15|Respiratory tuberculosis	2
A31.0|Pulmonary mycobacterial infection|Mycobacterium avium complex	3
A31.2|Disseminated mycobacterium avium-intracellulared complex (DMAC)|Disseminated infection with mycobacterium avium complex	4
A31.9|Mycobacterial infection, unspecified|Mycobacterium avium	5
A49.0|Staphylococcal infection, unspecified site	6
A69.20|Lyme disease, unspecified	7
B02.21|Postherpetic geniculate ganglionitis|Ramsey Hunt Syndrome	8
B20|Human Immunodeficiency virus [HIV] disease	9
B25|Cytomegalovirus disease	10
B27.90|Infectious mononucleosis, unspecified without complication	11
B38.9|Coccidioidomycosis, unspecified	12
B39.9|Histoplasmosis, unspecified	13
B44.9|Aspergillosis, unspecified	14
B45|Cryptococcosis, unspecified|Cryptococcal meningitis	15
B55.1|Cutaneous leishmaniasis	16
B55.2|Mucocutaneous leishmaniasis	17
B55.9|Leishmaniasis, unspecified	18
B69|Cysticercosis	19
B69.0|Cysticercosis of central nervous system|Neurocysricercosis	20
B85.2|Mediastinal (thymic) large B-cell lymphoma	21
C02.1|Malignant neoplasm of border of tongue|WOOT Trial Allen	22
C03.9|Malignant neoplasm of gum, unspecified|Alveolar soft palate sarcoma	23
C06.0|Malignant neoplasm of cheek mucosa|Mucosal melanoma	24
C09.9|Malignant neoplasm of tonsil, unspecified|Head and neck (tonsillar);Parotid tumor	25
C15.9|Malignant neoplasm of esophagus, unspecified	26
C16.0|Malignant neoplasm of cardia|Gastric cancer	27
C16.2|Malignant neoplasm of stomach|Stomach cancer	28
C17.0|Malignant neoplasm of duodenum|Adenocarcinoma	29
C18.9|Malignant neoplasm of colon, unspecified	30
C21.0|Malignant neoplasm of anus, unspecified	31
C22.0|Liver cell carcinoma	32
C22.1|Intrahepatic bile duct carcinoma	33
C22.8|Malignant neoplasm of liver, primary, unspecified|Hepatoblastoma	34
C25.3|Malignant neoplasm of pancreatic duct|Pancreatic cancer	35
C32.3|Malignant neoplasm of laryngeal cartilage	36
C34.0|Malignant neoplasm of main bronchus	37
C34.90|Malignant neoplasm of unspecified part of unspecified bronchus or lung|Cisplatin, Non small cell lung cancer	38
C34.91|Malignant neoplasm of unspecified part of right bronchus or lung|SCLC	39
C37|Malignant neoplasm of thymus|Thymoma	40
C41.4|Malignant neoplasm of pelvic bones/sacrum/coccyx|Bone cancer	41
C41.9|Malignant neoplasm of bone and articular cartilage, unspecified|Ewings Sarcoma	42
C43|Malignant melanoma	43
C44.2|Squamous cell carcinoma of skin, unspecified	44
C45.9|Mesothelioma, unspecified	45
C46.9|Kaposi's sarcoma, unspecified	46
C48.2|Malignant neoplasm of peritoneum, unspecified|Desmoplastic Small Round Sarcoma	47
C49.22|Malignant neoplasm of connective and soft tissue of left lower limb, including hip|Leiomyosarcoma	48
C49.4|Malignant neoplasm of connective and soft tissue of abdomen	49
C49.9|Malignant neoplasm of connective and soft tissue, unspecified	50
C50.9|Malignant neoplasm of breast, unspecified site	51
C53.9|Malignant neoplasm of cervix uteri, unspecified	52
C54.9|Malignant neoplasm of corpus uteri, unspecified|except isthmus	53
C56.9|Malignant neoplasm of unspecified ovary	54
C60.1|Malignant neoplasm of glans penis	55
C61|Malignant neoplasm of prostate	56
C62.9|Malignant neoplasm of testis, unspecified whether descended or undescended	57
C64|Malignant neoplasm of kidney, except renal pelvis|WAGR syndrome	58
C64.9|Malignant neoplasm of unspecified kidney, except renal pelvis	59
C65.2|Malignant neoplasm of left renal pelvis	60
C67.9|Malignant neoplasm of bladder	61
C69.90|Malignant neoplasm of unspecified site of unspecified eye|Ocular melanoma	62
C71.6|Malignant neoplasm of cerebellum|Medulloblastoma	63
C71.7|Malignant neoplasm of brain stem|Pontine Glioma;Glioma, DIPG	64
C71.9|Malignant neoplasm of brain, unspecified|Astrocytoma	65
C73|Malignant neoplasm of thyroid gland	66
C74|Malignant neoplasm of adrenal gland|Neuroblastoma	67
C74.90|Malignant neoplasm of unspecified part of unspecified adrenal gland	68
C75.1|Malignant neoplasm of pituitary gland	69
C75.3|Malignant neoplasm of pineal gland	70
C79|Secondary malignant neoplasm of other and unspecified sites|Metastatic sarcoma (knee,pancreas,lung)	71
C7A.00|Malignant carcinoid tumor of unspecified site	72
C81.90|Hodgkin lymphoma, unspecified, unspecified site	73
C82.00|Follicular lymphoma|Follicular lymphoma;Nodular lymphoma	74
C83.00|Small cell B-cell lymphoma, unspecified site|Small cell lung cancer	75
C83.18|Mantle cell lymphoma, lymph nodes of multiple sites|Mantle cell lymphoma	76
C83.30|Diffuse large B-cell lymphoma, unspecified site|Lymphoma;Diffuse large B-cell lymphoma	77
C83.8|Other non-follicular lymphoma|lymphomatoid granulomatosis [LYG]	78
C84.00|Mycosis fungoides|Peripheral T cell lymphoma;Cutaneous T cell lymphoma	79
C84.40|Peripheral T cell lymphoma|Peripheral T cell lymphoma	80
C84.70|Anaplastic large cell lymphoma, ALK-negative, unspecified site|Anaplastic large cell lymphoma	81
C85.89|Other specified types of non-Hodgkin lymphoma, extranodal and solid organ sites|Peripheral T-cell lymphoma	82
C85.90|Non-Hodgkin lymphoma, unspecified, unspecified site	83
C86.1|Hepatosplenic咭cell嫹mphoma|T-cell lymphoma	84
C86.4|Blastic NK-cell lymphoma|Plasmacytoid dendridic cell leukemi	85
C88.0|Waldenstorm Macroglobulinemia	86
C90.0|Multiple myeloma	87
C91.00|Acute lymphoblastic leukemia	88
C91.1|Chronic lymphocytic leukemia of B-cell type	89
C91.4|Hairy cell leukemia	90
C92.0|Acute myeloblastic leukemia	91
C93.1|Chronic myelomonocytic leukemia	92
D13.7|Benign neoplasm of endocrine pancreas|Insulinoma	93
D23.9|Other benign neoplasm of skin, unspecified|Birt-Hugg-Dube Syndrome	94
D32.9|Benign neoplasm of meninges, unspecified|Meningioma	95
D35.00|Benign neoplasm of unspecified adrenal gland|Pheochromocytoma	96
D35.6|Benign neoplasm of aortic body and other paraganglioma|Paraganglioma	97
D37.3|Neoplasm of uncertain behavior of appendix|Neuroendocrine Tumor	98
D46.9|Myelodysplastic syndrome, unspecified|Anaplastic thyroid cancer	99
D47.0|Mast cell neoplasms of uncertain behavior|Mastocytosis	100
D47.01|Cutaneous mastocytosis	101
D47.Z2|Castleman disease	102
D48.1|Neoplasm of uncertain behavior of connective and other soft tissue|Lymphangioleiomyomatosis	103
D51.2|Transcobalamin II Deficiency	104
D56.1|Beta thalassemia	105
D56.9|Thalassemia, unspecified	106
D57|Sickle-cell disorders	107
D61|Other aplastic anemias and other bone marrow failure syndromes|Shwachman Diamond Syndrome	108
D61.01|Constitutional (pure) red blood cell aplasia|Diamond Blackfan Anemia	109
D61.09|Other constitutional aplastic anemia|Fanconi Anemia	110
D61.8|Other specified aplastic anemias and other bone marrow failure syndromes|IBMFS	111
D61.81|Pancytopenia	112
D61.9|Aplastic anemia, unspecified	113
D64.9|Anemia, unspecified	114
D68.2|Hereditary deficiency of other clotting factors|GATA2	115
D69.42|Congenital and herediatry thrombocytopenia purpura|Thrombocytopenia Absent Radius	116
D70.9|Neutropenia, unspecified	117
D72.1|Eosinophilia	118
D72.119|Hypereosinophilic syndrome [HES], unspecified	119
D72.810|Lymphocytopenia|Lymphocytopenia	120
D76.1|Hemophagocytic lymphohistiocytosis|Macrophage Activation Syndrome [MAS]	121
D76.3|Other histiocytosis syndromes|Rosai dorfman syndrome	122
D80.0|Hereditary hypogammaglobulinemia|Agammaglobulinemia	123
D80.2|Selective deficiency of immunoglobulin A [IgA]	124
D81.2|Severe combined immunodeficiency [SCID] with low or normal B-cell numbers|CARD11 Deficiency	125
D81.3|Adenosine deaminase [ADA] deficiency	126
D81.31|Severe combined immunodeficiency due to adenosine deaminase deficiency|ADA-SCID	127
D81.8|Other combined immunodeficiencies|WHIM syndrome	128
D81.9|Combined immunodeficiency, unspecified	129
D82.0|Genetic anomalies of leukocytes|Leukocyte adhesion deficiency	130
D82.1|Di George's syndrome	131
D82.4|Hyperimmunoglobulin E [IgE]岹ndrome|Jobs syndrome	132
D83.9|Common variable immunodeficiency, unspecified	133
D84.1|Defects in the complement system|Chapel disease	134
D84.8|Other specified immunodeficiencies|Interferon Gamma Receptor Deficiency	135
D84.9|Immunodeficiency, unspecified	136
D85.5|Immunodeficiency with increased immunoglobulin M [IgM]	137
D86.9|Sarcoidosis, unspecified	138
D89.81|Graft-versus-host disease	139
D89.82|Autoimmune Lymphoproliferative syndrome [ALPS]	140
D89.89|Other specified disorders involving the immune mechanism, not elsewhere classified|APCED	141
D89.9|Disorder involving the immune mechanism, unspecified	142
E03.9|Hypothyroidism, unspecified	143
E05.00|Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm|Graves disease	144
E05.90|Thyrotoxicosis, unspecified without thyrotoxic crisis or storm|Graves disease	145
E07.9|Disorder of thyroid, unspecified	146
E10.8|Type 1 diabetes mellitus with unspecified complications|Diabetic retinopathy	147
E11.9|Type 2 diabetes mellitus without complications|Diabetes Mellitus	148
E13.40|Other specified diabetes mellitus with diabetic neuropathy, unspecified	149
E20.9|Hypoparathyroidism, unspecified|GATA3	150
E22.0|Acromegaly and pituitary gigantism|Acromegaly	151
E23.0|Hypopituitarism|Kallman's Syndrome	152
E23.3|Hypothalamic dysfunction, not elsewhere classified|Hypothalamic Amenorrhea	153
E23.7|Disorder of pituitary gland, unspecified|Pituitary Tumor	154
E23.9|Degenerative diseases of the basal ganglia|Corticobasal syndrome	155
E24.8|Other Cushing's syndrome	156
E25.0|Congenital adrenogenital disorders associated with enzyme deficiency|Congenital adrenal hyperplasia	157
E26.9|Hyperaldosteronism, unspecified	158
E27.8|Other spedcified disorders of adrenal gland|Adrenal hyperplasia	159
E27.9|Disorder of adrenal gland, unspecified|Adrenal deficiency	160
E29.1|Testicular hypofunction|Hypogonadotropic Hypogonadism	161
E31.0|Autoimmune polyglandular failure|IPEX syndrome	162
E31.21|Multiple endocrine neoplasia [MEN] type I	163
E31.22|Multiple endocrine neoplasia [MEN] type IIA	164
E34.0|Carcinoid syndrome	165
E38.4|Other specified endocrine disorders|Progeria	166
E40|Malignant neoplasm of bone and articular cartilage of limbs|Osteosarcoma	167
E70.29|Other disorders of tyrosine metabolism|Alkaptonuria	168
E70.32|Oculocutaneous albinism	169
E70.330|Chediak-Higashi syndrome	170
E70.331|Hermansky-Pudiak syndrome	171
E71.120|Methylmalonic acidemia|Combined melonic and methylmalonic acidemia	172
E71.121|Propionic acidemia	173
E72.04|Cystinosis|Fanconi syndrome	174
E72.8|Other specified disorders of amino-acid metabolism|Serine Deficiency	175
E74.0|Glycogen storage disease, unspecified	176
E74.02|Pompe disease	177
E74.89|Other specified disorders of carbohydrate metabolism|Congenital disorders of glycosylation	178
E75.01|Sandhoff disease	179
E75.02|Tay-Sachs Disease|GM2	180
E75.11|Mucolipidosis IV	181
E75.19|Other gangliosidosis|GM1	182
E75.21|Fabry (-Anderson) disease	183
E75.22|Gaucher's disease	184
E75.242|Neimann-Pick disease, type 2|HPBCD 	185
E75.25|Metachromatic leukodystrophy	186
E75.29|Other sphingolipidosis|Leukodystrophy	187
E75.4|Neuronal ceroid lipofuscinosis|CLN3	188
E75.5|Other lipid岴orage壩sorders|FSASD	189
E76.21|Morquio mucopolysaccharidoses, unspecified|Morquio syndrome	190
E77.1|Defects in glycoprotein degradation|Sialidosis	191
E77.8|Systemic involvement of connective tissue, unspecified|Connective tissue disorder syndrome [CTDS]	192
E78.00|Pure hypercholesterolemia, unspecified	193
E78.5|Hyperlipidemia, unspecified|Dyslipidemia	194
E78.6|Lipoprotein deficiency|Abetalipoproteinemia	195
E78.72|Smith-Lemli-Opitz syndrome	196
E83.01|Wilson's disease	197
E84.9|Cystic fibrosis, unspecified	198
E87.04|Cystinosis	199
E88.1|Lipodystrophy, not elsewhere classified|Lipodystrophy	200
E88.40|Mitochondrial metabolism disorder, unspecified|Mitochondrial disorder;Mitochondrial genetic disorder;Metabolic disorder;Mitochondrial disease;Mitochondrial complex I deficiency	201
E88.41|MELAS syndrome	202
E88.49|Other mitochondrial metabolism disorders|Mitochondrial DNA depletion syndrome;Mitochondrial complex III deficiency	203
E88.81|Dysmetabolic syndrome X|Metabolic syndrome	204
E88.89|Other specified metabolic disorders|Erdheim-Chester	205
E88.9|Metabolic壩sorder, unspecified|Inborn Metabolism Errors	206
F03|Unspecified dementia	207
F10.20|Alcohol depencence, uncomplicated	208
F20|Schizophrenia	209
F31.9|Bipolar disorder, unspecified	210
F32.A|Depression, unspecified	211
F34.8|Other persistent mood [affective] disorders|Mood Swings, Mid-Life Related	212
F43.10|Post-traumatic stress disorder, unspecified	213
F80.1|Expressive language disorder|Foreign Accent Syndrome	214
F80.81|Childhood history fluency disorder|Familial stuttering	215
F80.9|Developmental disorder of speech and language, unspecified	216
F84.0|Autistic disorder	217
F84.3|Other childhood disintegrative disorder|Childhood psychosis	218
F95.2|Tourette disorder	219
G03.2|Benign recurrent meningitis [Mollaret]|HSV meningitis	220
G03.8|Meningitis due to other specified causes|Fungal brain infection	221
G03.9|Meningitis, unspecified	222
G04.90|Encephalitis and encephalomyelitis, unspecified	223
G11.1|Friedreich ataxia	224
G11.4|Hereditary spastic paraplegia	225
G11.8|Other hereditary ataxias|Spinocerebellar ataxia, type 7	226
G12.1|Other inherited spinal muscular atrophy|Brown Vialetto Syndrome	227
G12.23|Primary lateral sclerosis	228
G14.8|Genetic carrier of other disease|GNAI2 Mutation	229
G20|Parkinson's disease	230
G24.5|Blepharospasm	231
G24.9|Dystonia, unspecified|Dystonia TMS Study	232
G25.3|Myoclonus	233
G25.9|Extrapyramidal and movement disorder, unspecified	234
G31.82|Leigh's disease|Leigh's syndrome	235
G31.9|Degenerative disease of nervous syndrome, unspecified|cerebellar degeneration	236
G35|Multiple sclerosis	237
G40.0|Epilepsy, unspecified	238
G51.0|Bell's Plasy	239
G60.0|Hereditary motor and sensory neuropathy|Charcot Marie Tooth	240
G60.8|Other hereditary and idiopathic neuropathies|Giant Axonal Neuropathy	241
G60.9|Hereditary and idiopathic孥uropathy, unspecified|Familial neuropathy	242
G61.82|Multifocal motor neuropathy	243
G62|Other and unspecified polyneuropathies|Sensory Neuropathy	244
G62.9|Polyneuropathy, unspecified|Peripheral Neuropathy	245
G71.0|Muscular dystrophy	246
G71.02|Facioscapulohumeral muscular dystrophy|Facioscapulohumeral muscular dystrophy-2嚆SHD2]	247
G71.3|Mitochondrial myopathy, not elsewhere specified|Mitochondrial myopathy	248
G72.9|Myopathy, unspecified	249
G76.0|Malignant neoplasm of head, face and neck	250
G93.40|Encephalopathy, unspecified	251
G95.0|Syringomyelia or syringobulbia|syringomyelia	252
G96.9|Disorder of central nervous system, unspecified |Neurosarcoidosis	253
H15.099|Other scleritis, unspecified eys	254
H16.32|Diffuse interstitial keratitis|Cogan syndrome	255
H20.00|Unspecified acute and subacute iridocyclitis|Granulomatous Uveitis	256
H20.823|Vogt Koyanagi Syndrome	257
H30.109|Unspecified disseminated chorioretinal inflammation, unspecified eye|Chorioretinitus	258
H35|Other retinal disorders|Retinal Dystrophy	259
H35.06|Retinal vasculitis	260
H35.52|Pigmentary retinal dystrophy|Retinitis pigmentosa	261
H35.53|Other dystrophies primarily involving the sensory retina|Cone Rod Dystrophy, Crolibulin+Cisplatin	262
H35.54|Dystrophies primarily involving the retinal pigment epithelium|Vitelliform dystrophy;Leber Congenital Amaurosis	263
H44.119|Panuveitis, unspecified eye	264
H44.13|Symoathetic uveitis	265
H47.099|Other disorders of optic nerve, not elsewhere classified, unspecified eye|Optic nerve atrophy	266
H47.9|Unspecified speech disturbances	267
H49.819|Kearns-Sayre syndrome, unspecified eye|Kearns-Sayre syndrome	268
H52.31|Anisometropia	269
H53.009|Unspecified amblyopia, unspecified eye	270
H55.0|Unspecified nystagmus	271
H66.9|Otitis media, unspecified	272
H71.90|Unspecified cholesteatoma, unspecified ear	273
H72.9|Unspecified perforation of tympanic membrane	274
H81.0|Meniere's disease	275
H81.39|Other peripheral vertigo	276
H90.3|Sensorineural hearing loss, bilateral|Autosomal dominant nonsyndromic, DFNA	277
H90.5|Unspecified sensorineural hearing loss	278
H91.09|Ototoxic hearing loss, unspecified ear	279
H91.9|Unspecified hearing loss|Deafness	280
H91.90|Unspecified hearing loss, unspecified ear	281
H91.93|Unspecified hearing loss, bilateral	282
H93.1|Tinnitus	283
H93.3|Disorders of acoustic nerve|acoustic neuroma	284
I63.9|Cerebral infaction, unspecified	285
I67|Other cerebrovascular diseases|Susac syndrome	286
I69.320|Aphasia following cerebral infarction	287
I71.0|Dissection of aorta|Loeys Dietz syndrome	288
I72|Other aneurysm |Basilar artery aneurysm	289
I89.8|Other specified noninfective disorders of lymphatic vessels and lymph nodes|Central conducting lymphatic anomaly	290
J20.9|Acute bronchitis, unspecified	291
J45.90|Unspecified asthma	292
J47.9|Bronchiectasis, uncomplicated	293
J84.89|Other specified interstitial pulmonary diseases|Bronchiolitis Obliterans Organizing Syndrome	294
J93.9|Pneumothorax, unspecified	295
K75.9|Inflammatory liver disease, unspecified|Hepatitis B	296
K76.89|Other specified diseases of liver|Nodular Regenerative Hyperplasia	297
L02.211|Cutaneous abscess of abdominal wall	298
L67.8|Other hair color and hair shaft abnormalities|Trichothiodystrophy	299
L92.9|Granulomatous disorder of the skin and subcutaneous tissue, unspecified|Chronic granulomatous disease	300
M04|Autoinflammatory syndrome	301
M04.1|Periodic Fever Syndromes|Familial cold autoinflammatory syndrome	302
M04.2|Cryopyrin-associated periodic syndromes|Muckle Wells syndrome	303
M04.8|Other autoinflammatory syndromes|CANDLE syndrome	304
M06.1|Adult-onset Stills disease	305
M06.9|Rheumatoid arthritis, unspecified	306
M11.2|Other chondrocalcinosis|Familial Tumoral Calcinosis	307
M13.0|Polyarthritis, unspecified	308
M22.2|Patellofemoral disorders|Patellofemoral syndrome [PFS]	309
M31.3|Wegener's granulomatosis	310
M31.30|Wegener's granulomatosis without renal involvement|GPA Vasculitis	311
M32|systemic lupus erythematosus	312
M33.1|Other dermamyositis	313
M35.2|Behcets disease	314
M35.8|Other specified systemic involvement of connective tissue|SAVI {STING}	315
M45|Ankylosing spondylitis	316
M60.9|Myositis, unspecified	317
M62.9|Disorder of muscle, unspecified|Congential hypotonia	318
M85.00|Fibrous displasia (monostotic), unspecified site	319
M86.3|Chronic multifocal osteomyelitis|SAPHO	320
M86.30|Chronic multifocal osteomyelitis, unspecified site	321
M88.9|Osteitis deformans of unspecified bone|Paget's disease	322
M90.80|Osteopathy in diseases classified elsewhere, unspecified site|Hypophosphatemic Rickets	323
M94.1|Relapsing Polychondritis	324
MO4.2|Cryopyrin associated periodic fever syndrome|5 year NOMID	325
N04.1|Nephrotic syndrome with focal and segmental glomerular lesions|Glomerulosclerosis	326
Q04.2|Holoprosencephaly	327
Q04.3|Other reduction deformities of brain|Joubert syndrome	328
Q07.0|Arnold-Chiari syndrome|Chiari 	329
Q11.2|Microphthalmos|Bosma Arhinia Microphthalmia	330
Q13.0|Coloboma of iris	331
Q13.1|Absence of iris|Aniridia	332
Q13.4|Other congenital corneal malformations|Peters anomaly	333
Q16.5|Congenital malformation of inner ear|Enlarged Vestibular Aqueduct [EVA]	334
Q18.4|Macrostomia|Ablepharon Macrostomia Syndrome	335
Q28.8|Other specified congenital malformations of circulatory system|Generalized arterial calcification of infancy [GACI]	336
Q34.8|Other specified congenital malformations of respiratory system|Kartagener's Syndrome	337
Q51.0|Agenesis and aplasia of uterus|Mayer-Rokitansky-Kuster-Hauser Syndrome	338
Q74.3|Arthrogryposis multiplex congenita|PIEZO2	339
Q75.4|Mandibulofacial dystosis|Treacher-Collins syndrome	340
Q77.7|Spondyloepiphyseal dysplasia	341
Q78.0|Osteogenesis imperfecta	342
Q78.2|Osteopetrosis	343
Q78.4|Enchondromatosis|Maffucci syndrome	344
Q78.5|Metaphyseal dysplasia|Jansen's Metaphyseal Chrondroplasia	345
Q78.8|Other specified osteochondrodysplasias|Saul Wilson Disease	346
Q79.6|Ehlers-Danlos syndrome	347
Q79.8|Other disorders of aromatic amino acid metabolism|Waardenburg syndrome	348
Q79.9|Congenital malformation of musculoskeletal system, unspecified|Skeletal Dysplasia	349
Q80.9|Congenital ichthyosis, unspecified	350
Q82.1|Xeroderma pigmentosum|Xeroderma pigmentosum	351
Q82.8|Other specified congenital malformations of skin|Dyskeratosis Congenita	352
Q85.01|Neurofibromatosis, type 1|APD Study	353
Q85.02|Neurofibromatosis, type 2 (acoustic neurofibromatosis)	354
Q85.8|Other phakomatoses, not otherwise classified|Von Hippel Lindau Disease	355
Q87.0|Congenital malformation syndromes predominantly affecting facial appearance|Greig syndrome	356
Q87.1|Polyostotic fibrous dysplasia|McCune albright syndrome	357
Q87.19|Other congenital malformation syndromes predominantly associated with short stature|Cockayne syndrome;Noonan Syndrome	358
Q87.2|Congenital malformatin syndromes predominantly involving limbs|VACTERL Association	359
Q87.3|Congenital malformation syndromes involving early overgrowth|Cloves syndrome	360
Q87.8|Other specified congenital malformation syndromes, not elsewhere classified|Costello syndrome	361
Q87.89|Other specified congneital malformation syndromes, not otherwise classified|Bardet-Biedl Syndrome	362
Q89.7|Multiple congenital malformations, not elsewhere classified|Carney Complex	363
Q89.8|Other specified congenital malformations|Alstrom syndrome	364
Q90.9|Down syndrome, unspecified	365
Q93.5|Other deletions of part of a chromosome|Phelan-McDermid Syndrome	366
Q93.51|Angelman syndrome	367
Q93.82|William's syndrome	368
Q93.88|Other microdeletions|Smith-Magenis Syndrome	369
Q96.9|Turner's syndrome, unspecified	370
Q98.0|Klinefelter syndrome karyotype 47, XXY	371
Q99.8|Other specified chromosome abnormalities	372
Q99.9|Chromosomal abnormality, unspecified|Sex chromosome abnormality	373
R25.0|Abnormal head movements|Head Nodding Syndrome	374
R27.0|Ataxia, unspecified	375
R41.9|Unspecified symptoms and signs involving cognitive functions and awareness|Cognitive impairment	376
R42|Dizziness and giddiness|Mal De Debarquement syndrome	377
R47.01|Aphasia	378
R53.82|Chronic fatigue, unspecified|chronic fatigue syndrome	379
R62|Lack of expected normal physiological development in childhood and adults|Failure To Thrive	380
R62.50|Unspecified lack of expected normal physiological development in childhood	381
R62.52|Short stature [child]	382
R80|Proteinuria	383
S06.2|Diffuse traumatic brain injury	384
T78.40|Allergy, unspecified	385
U09.9|Post COVID-19 condition, unspecified|Post COVID Tinnitus	386
Z13.29|Encounter for screening for other suspected endocrine disorder	387
Z13.79|Encounter for other screening for genetic and chromosomal anomalies	388
Z15|Genetic susceptibility to disease|Li-Fraumeni Syndrome, Family History	389
Z15.09|Genetic susceptibility to other malignant neoplasm|CHD1 mutation	390
Z15.89|Genetic susceptibility to other disease|Germline Runx1 Mutation	391
Z20.810|Contact with and (suspected) exposure to anthrax	392
Z82.2|Family history of deafness and hearing loss|Autosomal dominant nonsyndromic, DFNA, family	393
Z94.81|Bone marrow transplant status	394
