ClinicalGroup_ID ICD-10 code ICD-10 descriptor Modifiers 162001 A15 Respiratory tuberculosis 947001 A31.0 Pulmonary mycobacterial infection Mycobacterium avium complex 119001 A31.0 Pulmonary mycobacterial infection 945001 A31.0 Pulmonary mycobacterial infection Pulmonary nontuberculosis mycobacterium 272001 A31.2 Disseminated mycobacterium avium-intracellulared complex (DMAC) Disseminated infection with mycobacterium avium complex 58001 A31.9 Mycobacterial infection, unspecified Mycobacterium avium 427001 A31.9 Mycobacterial infection, unspecified 719001 A49.0 Staphylococcal infection, unspecified site 395001 A69.20 Lyme disease, unspecified 732001 B02.21 Postherpetic geniculate ganglionitis Ramsey Hunt Syndrome 181001 B20 Human Immunodeficiency virus [HIV] disease 13001 B20 Human immunodeficiency virus [HIV] disease 49001 B25 Cytomegalovirus disease 1033001 B27.90 Infectious mononucleosis, unspecified without complication 927001 B38.9 Coccidioidomycosis, unspecified 593001 B39.9 Histoplasmosis, unspecified 884001 B44.9 Aspergillosis, unspecified 1050001 B45 Cryptococcosis, unspecified Cryptococcal meningitis 758001 B45 Cryptococcosis, unspecified Cryptococcal meningitis 815001 B55.1 Cutaneous leishmaniasis 858001 B55.2 Mucocutaneous leishmaniasis 1057001 B55.9 Leishmaniasis, unspecified 53001 B69 Cysticercosis 865001 B69.0 Cysticercosis of central nervous system Neurocysricercosis 528001 B85.2 Mediastinal (thymic) large B-cell lymphoma 1096001 C02.1 Malignant neoplasm of border of tongue WOOT Trial Allen 290001 C15.9 Malignant neoplasm of esophagus, unspecified 238001 C18.9 Malignant neoplasm of colon, unspecified 1074001 C22.0 Liver cell carcinoma 384001 C32.3 Malignant neoplasm of laryngeal cartilage 95001 C34.0 Malignant neoplasm of main bronchus 574001 C34.90 Malignant neoplasm of unspecified part of unspecified bronchus or lung Cisplatin, Non small cell lung cancer 827001 C34.90 Malignant neoplasm of unspecified part of unspecified bronchus or lung Non-small cell lung cancer 913001 C37 Malignant neoplasm of thymus Thymoma 64001 C41.9 Malignant neoplasm of bone and articular cartilage, unspecified Ewings Sarcoma 102001 C43 Malignant melanoma 152001 C44.2 Squamous cell carcinoma of skin, unspecified 650001 C45.9 Mesothelioma, unspecified 378001 C46.9 Kaposi's sarcoma, unspecified 261001 C48.2 Malignant neoplasm of peritoneum, unspecified Desmoplastic Small Round Sarcoma 141001 C49.4 Malignant neoplasm of connective and soft tissue of abdomen 140001 C49.9 Malignant neoplasm of connective and soft tissue, unspecified 33001 C50.9 Malignant neoplasm of breast, unspecified site 118001 C56.9 Malignant neoplasm of unspecified ovary 129001 C61 Malignant neoplasm of prostate 1024001 C62.9 Malignant neoplasm of testis, unspecified whether descended or undescended 661001 C64 Malignant neoplasm of kidney, except renal pelvis WAGR syndrome 104001 C64.9 Malignant neoplasm of unspecified kidney, except renal pelvis 744001 C67.9 Malignant neoplasm of bladder 114001 C69.90 Malignant neoplasm of unspecified site of unspecified eye Ocular melanoma 467001 C71.7 Malignant neoplasm of brain stem Pontine Glioma 101001 C71.6 Malignant neoplasm of cerebellum Medulloblastoma 1047001 C71.7 Malignant neoplasm of brain stem Glioma, DIPG 23001 C71.9 Malignant neoplasm of brain, unspecified Astrocytoma 210001 C71.9 Malignant neoplasm of brain, unspecified 32001 C71.9 Malignant neoplasm of brain, unspecified Brainstem glioma 284001 C71.9 Malignant neoplasm of brain, unspecified Ependynoma 315001 C71.9 Malignant neoplasm of brain, unspecified Glioblastoma multiforme 318001 C71.9 Malignant neoplasm of brain, unspecified Glioblastoma 75001 C71.9 Malignant neoplasm of brain, unspecified Glioma 529001 C73 Malignant neoplasm of thyroid gland 435001 C74 Malignant neoplasm of adrenal gland Neuroblastoma 176001 C74.90 Malignant neoplasm of unspecified part of unspecified adrenal gland 787001 C75.1 Malignant neoplasm of pituitary gland 637001 C75.3 Malignant neoplasm of pineal gland 83001 C81.90 Hodgkin lymphoma, unspecified, unspecified site 97001 C83.8 Other non-follicular lymphoma lymphomatoid granulomatosis [LYG] 397001 C85.90 Non-Hodgkin lymphoma, unspecified, unspecified site 112001 C85.90 Non-Hodgkin lymphoma, unspecified, unspecified site 685001 C88.0 Waldenstorm Macroglobulinemia 423001 C90.0 Multiple myeloma 107001 C90.0 Multiple myeloma 34001 C91.00 Acute lymphoblastic leukemia 944001 C91.00 Acute lymphoblastic leukemia 41001 C91.1 Chronic lymphocytic leukemia of B-cell type 587001 C91.4 Hairy cell leukemia 189001 C92.0 Acute myeloblastic leukemia 42001 C93.1 Chronic myelomonocytic leukemia 736001 D13.7 Benign neoplasm of endocrine pancreas Insulinoma 976001 D23.9 Other benign neoplasm of skin, unspecified Birt-Hugg-Dube Syndrome 724001 D32.9 Benign neoplasm of meninges, unspecified Meningioma 463001 D35.00 Benign neoplasm of unspecified adrenal gland Pheochromocytoma 626001 D35.6 Benign neoplasm of aortic body and other paraganglioma Paraganglioma 1094001 D37.3 Neoplasm of uncertain behavior of appendix Neuroendocrine Tumor 916001 D46.9 Myelodysplastic syndrome, unspecified Anaplastic thyroid cancer 428001 D46.9 Myelodysplastic syndrome, unspecified 760001 D47.0 Mast cell neoplasms of uncertain behavior Mastocytosis 680001 D47.01 Cutaneous mastocytosis 1037001 D47.Z2 Castleman disease 785001 D51.2 Transcobalamin II Deficiency 213001 D56.1 Beta thalassemia 155001 D56.9 Thalassemia, unspecified 144001 D57 Sickle-cell disorders 498001 D61 Other aplastic anemias and other bone marrow failure syndromes Shwachman Diamond Syndrome 250001 D61.01 Constitutional (pure) red blood cell aplasia Diamond Blackfan Anemia 57001 D61.01 Constitutional (pure) red blood cell aplasia Diamond Blackfan Anemia 68001 D61.09 Other constitutional aplastic anemia Fanconi Anemia 367001 D61.8 Other specified aplastic anemias and other bone marrow failure syndromes IBMFS 448001 D61.81 Pancytopenia 20001 D61.9 Aplastic anemia, unspecified 190001 D64.9 Anemia, unspecified 767001 D68.2 Hereditary deficiency of other clotting factors GATA2 666001 D69.42 Congenital and herediatry thrombocytopenia purpura Thrombocytopenia Absent Radius 675001 D70.9 Neutropenia, unspecified 674001 Z00.6 Neutropenia, unspecified Neutropenia, unaffected family member 61001 D72.1 Eosinophilia 562001 D72.119 Hypereosinophilic syndrome [HES], unspecified 951001 D76.1 Hemophagocytic lymphohistiocytosis Macrophage Activation Syndrome [MAS] 1129001 D76.3 Other histiocytosis syndromes Rosai dorfman syndrome 179001 D80.0 Hereditary hypogammaglobulinemia Agammaglobulinemia 613001 D80.0 Hereditary hypogammaglobulinemia Bruton Disease 357001 D80.0 Hereditary hypogammaglobulinemia 550001 D80.0 Hereditary hypogammaglobulinemia X-linked Agammaglobulinemia 365001 D80.2 Selective deficiency of immunoglobulin A [IgA] 1035001 D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers CARD11 Deficiency 172001 D81.3 Adenosine deaminase [ADA] deficiency 1004001 D81.3 Adenosine deaminase [ADA] deficiency 495001 D81.31 Severe combined immunodeficiency due to adenosine deaminase deficiency ADA-SCID 687001 D81.8 Other combined immunodeficiencies WHIM syndrome 870001 D81.8 Other combined immunodeficiencies PI3K 748001 D81.9 Combined immunodeficiency, unspecified 962001 D81.9 Combined immunodeficiency, unspecified STAT1 deficiency 810001 D81.9 Combined immunodeficiency, unspecified DOCK8 immunodeficiency 941001 D81.9 Combined immunodeficiency, unspecified Gain of Function Stat1 91001 D82.0 Genetic anomalies of leukocytes Leukocyte adhesion deficiency 389001 D82.0 Genetic anomalies of leukocytes Leukocyte adhesion deficiency 652001 D82.1 Di George's syndrome 88001 D82.4 Hyperimmunoglobulin E [IgE]Êsyndrome Jobs syndrome 351001 D82.4 Hyperimmunoglobulin E [IgE] syndrome 819001 D83.9 Common variable immunodeficiency, unspecified 793001 D84.8 Other specified immunodeficiencies Interferon Gamma Receptor Deficiency 433001 D84.8 Other specified immunodeficiencies NEMO syndrome 780001 D84.8 Other specified immunodeficiencies IL12R Defect 894001 D84.8 Other specified immunodeficiencies ALPS due to CTLA4 mutation 370001 D84.9 Immunodeficiency, unspecified 539001 D84.9 Immunodeficiency, unspecified 1031001 D84.9 Immunodeficiency, unspecified SHARPIN 352001 D85.5 Immunodeficiency with increased immunoglobulin M [IgM] 584001 D86.9 Sarcoidosis, unspecified 600001 D89.81 Graft-versus-host disease 697001 D89.81 Graft-versus-host disease 197001 D89.82 Autoimmune Lymphoproliferative syndrome [ALPS] 590001 D89.9 Disorder involving the immune mechanism, unspecified 360001 E03.9 Hypothyroidism, unspecified 742001 E07.9 Disorder of thyroid, unspecified 84001 E20.9 Hypoparathyroidism, unspecified GATA3 7001 E22.0 Acromegaly and pituitary gigantism Acromegaly 376001 E23.0 Hypopituitarism Kallman's Syndrome 1061001 E23.3 Hypothalamic dysfunction, not elsewhere classified Hypothalamic Amenorrhea 726001 E23.7 Disorder of pituitary gland, unspecified Pituitary Tumor 568001 E23.9 Degenerative diseases of the basal ganglia Corticobasal syndrome 244001 E24.8 Other Cushing's syndrome 578001 E25.0 Congenital adrenogenital disorders associated with enzyme deficiency Congenital adrenal hyperplasia 718001 E26.9 Hyperaldosteronism, unspecified 654001 E27.8 Other spedcified disorders of adrenal gland Adrenal hyperplasia 966001 E27.9 Disorder of adrenal gland, unspecified Adrenal deficiency 738001 E29.1 Testicular hypofunction Hypogonadotropic Hypogonadism 373001 E31.0 Autoimmune polyglandular failure IPEX syndrome 1028001 E31.0 Autoimmune polyglandular failure Autoimmune polyendocrinopathy type 1 [APECED] 851001 E31.21 Multiple endocrine neoplasia [MEN] type I 1022001 E31.22 Multiple endocrine neoplasia [MEN] type IIA 657001 E34.0 Carcinoid syndrome 472001 E38.4 Other specified endocrine disorders Progeria 117001 E40 Malignant neoplasm of bone and articular cartilage of limbs Osteosarcoma 18001 E70.29 Other disorders of tyrosine metabolism Alkaptonuria 821001 E70.32 Oculocutaneous albinism 672001 E70.32 Oculocutaneous albinism 682001 E70.32 Oculocutaneous albinism 556001 E70.330 Chediak-Higashi syndrome 347001 E70.331 Hermansky-Pudiak syndrome 1090001 E71.120 Methylmalonic acidemia Combined melonic and methylmalonic acidemia 823001 E71.120 Methylmalonic acidemia Cobalamin C deficiency 1089001 E71.120 Methylmalonic acidemia Cobalamin A deficiency 414001 E71.120 Methylmalonic acidemia 996001 E71.121 Propionic acidemia 618001 E72.04 Cystinosis Fanconi syndrome 1009001 E72.8 Other specified disorders of amino-acid metabolism Serine Deficiency 320001 E74.0 Glycogen storage disease, unspecified 706001 E74.02 Pompe disease 855001 E74.89 Other specified disorders of carbohydrate metabolism Congenital disorders of glycosylation 1008001 E74.89 Other specified disorders of carbohydrate metabolism Congenital disorders of glycosylation 892001 E75.01 Sandhoff disease 740001 E75.02 Tay-Sachs Disease GM2 985001 E75.02 Tay Sachs Disease Late Onset Tay Sachs Disease 105001 E75.11 Mucolipidosis IV 688001 E75.19 Other gangliosidosis GM1 66001 E75.21 Fabry (-Anderson) disease 74001 E75.22 Gaucher's disease 313001 E75.22 Gaucher's disease 880001 E75.242 Neimann-Pick disease, type 2 HPBCD 110001 E75.242 Neimann-Pick disease, type 2 110001 E75.242 Neimann-Pick disease, type 2 94001 E75.25 Metachromatic leukodystrophy 1011001 E75.4 Neuronal ceroid lipofuscinosis CLN3 1018001 E75.4 Neuronal ceroid lipofuscinosis CLN3 751001 E75.4 Neuronal ceroid lipofuscinosis 957001 E76.21 Morquio mucopolysaccharidoses, unspecified Morquio syndrome 998001 E77.1 Defects in glycoprotein degradation Sialidosis 1016001 E77.8 Systemic involvement of connective tissue, unspecified Connective tissue disorder syndrome [CTDS] 789001 E78.00 Pure hypercholesterolemia, unspecified 806001 E78.5 Hyperlipidemia, unspecified Dyslipidemia 847001 E78.6 Lipoprotein deficiency Abetalipoproteinemia 387001 E78.6 Lipoprotein deficiency LCAT deficiency 146001 E78.72 Smith-Lemli-Opitz syndrome 717001 E83.01 Wilson's disease 615001 E84.9 Cystic fibrosis, unspecified 54001 E87.04 Cystinosis 103001 E88.41 MELAS syndrome 849001 E88.89 Other specified metabolic disorders Erdheim-Chester 371001 E88.9 MetabolicÊdisorder, unspecified Inborn Metabolism Errors 258001 F03 Unspecified dementia 9001 F10.20 Alcohol depencence, uncomplicated 16001 F20 Schizophrenia 31001 F31.9 Bipolar disorder, unspecified 259001 F32.A Depression, unspecified 417001 F34.8 Other persistent mood [affective] disorders Mood Swings, Mid-Life Related 476001 F43.10 Post-traumatic stress disorder, unspecified 630001 F80.1 Expressive language disorder Foreign Accent Syndrome 79001 F80.81 Childhood history fluency disorder Familial stuttering 255001 F80.9 Developmental disorder of speech and language, unspecified 801001 F80.9 Developmental disorder of speech and language, unspecified Language delay study 762001 F84.0 Autistic disorder 221001 F84.3 Other childhood disintegrative disorder Childhood psychosis 703001 F95.2 Tourette disorder 642001 G03.9 Meningitis, unspecified 1131001 G04.90 Encephalitis and encephalomyelitis, unspecified 72001 G11.1 Friedreich ataxia 777001 G11.4 Hereditary spastic paraplegia 1069001 G11.8 Other hereditary ataxias Spinocerebellar ataxia, type 7 669001 G11.8 Other hereditary ataxias Spinocerebellar ataxia, type 7 955001 G12.1 Other inherited spinal muscular atrophy Brown Vialetto Syndrome 612001 G12.23 Primary lateral sclerosis 1049001 G14.8 Genetic carrier of other disease GNAI2 Mutation 123001 G20 Parkinson's disease 624001 G24.5 Blepharospasm 803001 G24.9 Dystonia, unspecified Dystonia TMS Study 108001 G25.3 Myoclonus 418001 G25.9 Extrapyramidal and movement disorder, unspecified 36001 G31.9 Degenerative disease of nervous syndrome, unspecified cerebellar degeneration 63001 G35 Multiple sclerosis 756001 G40.0 Epilepsy, unspecified 286001 G40.0 Epilepsy, unspecified 494001 G40.0 Epilepsy, unspecified 295001 G51.0 Bell's Plasy 625001 G60.0 Hereditary motor and sensory neuropathy Charcot Marie Tooth 982001 G60.8 Other hereditary and idiopathic neuropathies Giant Axonal Neuropathy 862001 G60.9 Hereditary and idiopathicÊneuropathy, unspecified Familial neuropathy 918001 G61.82 Multifocal motor neuropathy 907001 G62 Other and unspecified polyneuropathies Sensory Neuropathy 455001 G62.9 Polyneuropathy, unspecified Peripheral Neuropathy 808001 G71.0 Muscular dystrophy 1015001 G71.02 Facioscapulohumeral muscular dystrophy Facioscapulohumeral muscular dystrophy-2Ê[FSHD2] 664001 G71.3 Mitochondrial myopathy, not elsewhere specified Mitochondrial myopathy 765001 G72.9 Myopathy, unspecified 1059001 G72.9 Myopathy, unspecified 15001 G76.0 Malignant neoplasm of head, face and neck 349001 G76.0 Malignant neoplasm of head, face and neck 776001 G93.40 Encephalopathy, unspecified 826001 G95.0 Syringomyelia or syringobulbia syringomyelia 142001 H15.099 Other scleritis, unspecified eys 47001 H16.32 Diffuse interstitial keratitis Cogan syndrome 911001 H20.00 Unspecified acute and subacute iridocyclitis Granulomatous Uveitis 137001 H20.823 Vogt Koyanagi Syndrome 620001 H30.109 Unspecified disseminated chorioretinal inflammation, unspecified eye Chorioretinitus 774001 H35 Other retinal disorders Retinal Dystrophy 621001 H35.06 Retinal vasculitis 136001 H35.52 Pigmentary retinal dystrophy Retinitis pigmentosa 48001 H35.53 Other dystrophies primarily involving the sensory retina Cone Rod Dystrophy, Crolibulin+Cisplatin 1076001 H35.54 Dystrophies primarily involving the retinal pigment epithelium Vitelliform dystrophy 449001 H44.119 Panuveitis, unspecified eye 164001 H44.13 Symoathetic uveitis 441001 H47.099 Other disorders of optic nerve, not elsewhere classified, unspecified eye Optic nerve atrophy 143001 H47.9 Unspecified speech disturbances 833001 H52.31 Anisometropia 648001 H53.009 Unspecified amblyopia, unspecified eye 923001 H55.0 Unspecified nystagmus 592001 H66.9 Otitis media, unspecified 224001 H71.90 Unspecified cholesteatoma, unspecified ear 533001 H72.9 Unspecified perforation of tympanic membrane 413001 H81.0 Meniere's disease 543001 H81.39 Other peripheral vertigo 25001 H90.3 Sensorineural hearing loss, bilateral Autosomal dominant nonsyndromic, DFNA 541001 H90.3 Sensorineural hearing loss, bilateral Usher syndrome 1124001 H90.3 Sensorineural hearing loss, bilateral Usher syndrome type I, CDH23 508001 H90.5 Unspecified sensorineural hearing loss 514001 H90.5 Unspecified sensorineural hearing loss 1111001 H90.5 Unspecifed sensorineural hearing loss Fluctuating sensorineural hearing loss SNHL 444001 H91.09 Ototoxic hearing loss, unspecified ear 839001 H91.09 Ototoxic hearing loss, unspecified ear 253001 H91.9 Unspecified hearing loss Deafness 336001 H91.90 Unspecified hearing loss, unspecified ear 339001 H91.90 Unspecified hearing loss, unspecified ear 341001 H91.90 Unspecified hearing loss, unspecified ear 342001 H91.90 Unspecified hearing loss, unspecified ear 340001 H91.93 Unspecified hearing loss, bilateral 531001 H93.1 Tinnitus 170001 H93.3 Disorders of acoustic nerve acoustic neuroma 987001 H93.3 Disorders of acoustic nerve acoustic neuroma 520001 I63.9 Cerebral infaction, unspecified 841001 I67 Other cerebrovascular diseases Susac syndrome 128001 I69.320 Aphasia following cerebral infarction 1043001 I71.0 Dissection of aorta Loeys Dietz syndrome 202001 I72 Other aneurysm Basilar artery aneurysm 585001 J20.9 Acute bronchitis, unspecified 22001 J45.90 Unspecified asthma 876001 J47.9 Bronchiectasis, uncomplicated 872001 J84.89 Other specified interstitial pulmonary diseases Bronchiolitis Obliterans Organizing Syndrome 843001 J93.9 Pneumothorax, unspecified 345001 K75.9 Inflammatory liver disease, unspecified Hepatitis B 82001 K75.9 Inflammatory liver disease, unspecified Hepatitis C 595001 K75.9 Inflammatory liver disease, unspecified Hepatitis D 1013001 K76.89 Other specified diseases of liver Nodular Regenerative Hyperplasia 167001 L02.211 Cutaneous abscess of abdominal wall 159001 L67.8 Other hair color and hair shaft abnormalities Trichothiodystrophy 37001 L92.9 Granulomatous disorder of the skin and subcutaneous tissue, unspecified Chronic granulomatous disease 632001 L92.9 Granulomatous disorder of the skin and subcutaneous tissue, unspecified Chronic granulomatous disease 227001 L92.9 Granulomatous disorder of the skin and subcutaneous tissue, unspecified Chronic granulomatous disease 750001 M04 Autoinflammatory syndrome 69001 M04.1 Periodic Fever Syndromes Familial cold autoinflammatory syndrome 308001 M04.1 Periodic Fever Syndromes Familial mediterranean fever syndrome 300001 M04.1 Periodic Fever Syndromes Familial mediterranean fever syndrome 70001 M04.1 Periodic Fever Syndromes 420001 M04.2 Cryopyrin-associated periodic syndromes Muckle Wells syndrome 782001 M04.8 Other autoinflammatory syndromes CANDLE syndrome 690001 M04.8 Other autoinflammatory syndromes DIRA 121001 M04.8 Other autoinflammatory syndromes PAPA syndrome 518001 M06.1 Adult-onset Stills disease 482001 M06.9 Rheumatoid arthritis, unspecified 303001 M11.2 Other chondrocalcinosis Familial Tumoral Calcinosis 580001 M13.0 Polyarthritis, unspecified 461001 M22.2 Patellofemoral disorders Patellofemoral syndrome [PFS] 548001 M31.3 Wegener's granulomatosis 920001 M31.30 Wegener's granulomatosis without renal involvement GPA Vasculitis 393001 M32 systemic lupus erythematosus 96001 M32 systemic lupus erythematosus 55001 M33.1 Other dermamyositis 29001 M35.2 Behcets disease 901001 M35.8 Other specified systemic involvement of connective tissue SAVI {STING} 1073001 M45 Ankylosing spondylitis 109001 M60.9 Myositis, unspecified 307001 M85.00 Fibrous displasia (monostotic), unspecified site 646001 M86.3 Chronic multifocal osteomyelitis SAPHO 713001 M86.30 Chronic multifocal osteomyelitis, unspecified site 446001 M88.9 Osteitis deformans of unspecified bone Paget's disease 693001 M90.80 Osteopathy in diseases classified elsewhere, unspecified site Hypophosphatemic Rickets 925001 M94.1 Relapsing Polychondritis 484001 M94.1 Relapsing polychondritis 1098001 M94.1 Relapsing polychondritis VEXAS 860001 MO4.2 Cryopyrin associated periodic fever syndrome 5 year NOMID 953001 MO4.2 Cryopyrin associated periodic fever syndrome 89001 MO4.2 Cryopyrin associated periodic fever syndrome NOMID 1071001 MO4.2 Cryopyrin associated periodic fever syndrome 10 year NOMID 71001 N04.1 Nephrotic syndrome with focal and segmental glomerular lesions Glomerulosclerosis 73001 N04.1 Nephrotic syndrome with focal and segmental glomerular lesions Focal segmental glomulerosclerosis [FSGS] 616001 Q04.2 Holoprosencephaly 728001 Q04.3 Other reduction deformities of brain Joubert syndrome 602001 Q07.0 Arnold-Chiari syndrome Chiari 868001 Q07.0 Arnold-Chiari syndrome Chiari 1026001 Q11.2 Microphthalmos Bosma Arhinia Microphthalmia 416001 Q11.2 Microphthalmos 236001 Q13.0 Coloboma of iris 704001 Q13.1 Absence of iris Aniridia 721001 Q13.4 Other congenital corneal malformations Peters anomaly 26001 Q16.5 Congenital malformation of inner ear Enlarged Vestibular Aqueduct [EVA] 874001 Q18.4 Macrostomia Ablepharon Macrostomia Syndrome 896001 Q28.8 Other specified congenital malformations of circulatory system Generalized arterial calcification of infancy [GACI] 835001 Q34.8 Other specified congenital malformations of respiratory system Kartagener's Syndrome 970001 Q34.8 Other specified congenital malformations of respiratory system Primary Ciliary Dyskenesia 635001 Q51.0 Agenesis and aplasia of uterus Mayer-Rokitansky-Kuster-Hauser Syndrome 1006001 Q74.3 Arthrogryposis multiplex congenita PIEZO2 990001 Q75.4 Mandibulofacial dystosis Treacher-Collins syndrome 889001 Q77.7 Spondyloepiphyseal dysplasia 115001 Q78.0 Osteogenesis imperfecta 610001 Q78.2 Osteopetrosis 1114001 Q78.4 Enchondromatosis Maffucci syndrome 1118001 Q78.4 Enchondromatosis Ollier's disease 1122001 Q78.5 Metaphyseal dysplasia Jansen's Metaphyseal Chrondroplasia 1041001 Q78.8 Other specified osteochondrodysplasias Saul Wilson Disease 633001 Q79.6 Ehlers-Danlos syndrome 754001 Q79.8 Other disorders of aromatic amino acid metabolism Waardenburg syndrome 899001 Q79.9 Congenital malformation of musculoskeletal system, unspecified Skeletal Dysplasia 662001 Q80.9 Congenital ichthyosis, unspecified 551001 Q82.1 Xeroderma pigmentosum Xeroderma pigmentosum 273001 Q82.8 Other specified congenital malformations of skin Dyskeratosis Congenita 798001 Q85.01 Neurofibromatosis, type 1 APD Study 582001 Q85.01 Neurofibromatosis, type 1 111001 Q85.02 Neurofibromatosis, type 2 (acoustic neurofibromatosis) 796001 Q85.02 Neurofibromatosis, type 2 (acoustic neurofibromatosis) Small VS 978001 Q85.02 Neurofibromatosis, type 2 (acoustic neurofibromatosis) Small VS 280001 Q85.8 Other phakomatoses, not otherwise classified Von Hippel Lindau Disease 708001 Q85.8 Other phakomatoses, not otherwise classified Von Hippel Lindau Disease 165001 Q85.8 Other phakomatoses, not otherwise classified Von Hippel Lindau Disease 77001 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Greig syndrome 715001 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Moebius syndrome 422001 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Muenke syndrome 932001 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Pitt-Hopkins Syndrome 656001 Q87.0 Congenital malformation syndromes predominantly affecting facial appearance Freeman sheldon syndrome 100001 Q87.1 Polyostotic fibrous dysplasia McCune albright syndrome 46001 Q87.19 Other congenital malformation syndromes predominantly associated with short stature Cockayne syndrome 857001 Q87.19 Other congenital malformation syndromes predominantly associated with short stature Dubowitz syndrome 710001 Q87.2 Congenital malformatin syndromes predominantly involving limbs VACTERL Association 905001 Q87.3 Congenital malformation syndromes involving early overgrowth Cloves syndrome 120001 Q87.3 Congenital malformation syndromes involving early overgrowth Pallister Hall Syndrome 130001 Q87.3 Congenital malformation syndromes involving early overgrowth Proteus syndrome 1116001 Q87.8 Other specified congenital malformation syndromes, not elsewhere classified Costello syndrome 1084001 Q87.8 Other specified congenital malformation syndromes, not elsewhere classified Desmosterolosis 1120001 Q87.8 Other specified congenital malformation syndromes, not elsewhere classified LRP2 mutation 410001 Q87.8 Other specified congenital malformation syndromes, not elsewhere classified McKusick-Kaufman 597001 Q87.8 Other specified congenital malformation syndromes, not elsewhere classified MURCS Association 200001 Q87.89 Other specified congneital malformation syndromes, not otherwise classified Bardet-Biedl Syndrome 35001 Q89.7 Multiple congenital malformations, not elsewhere classified Carney Complex 186001 Q89.8 Other specified congenital malformations Alstrom syndrome 822001 Q89.8 Other specified congenital malformations Stickler syndrome 695001 Q90.9 Down syndrome, unspecified 903001 Q93.5 Other deletions of part of a chromosome Phelan-McDermid Syndrome 943001 Q93.51 Angelman syndrome 1067001 Q93.82 William's syndrome 148001 Q93.88 Other microdeletions Smith-Magenis Syndrome 502001 Q93.88 Other microdeletions Smith-Magenis Syndrome 163001 Q96.9 Turner's syndrome, unspecified 90001 Q98.0 Klinefelter syndrome karyotype 47, XXY 980001 Q99.9 Chromosomal abnormality, unspecified Sex chromosome abnormality 853001 Q99.9 Chromosomal abnormality, unspecified Y-Chromosome variant 878001 R25.0 Abnormal head movements Head Nodding Syndrome 24001 R27.0 Ataxia, unspecified 1106001 R41.9 Unspecified symptoms and signs involving cognitive functions and awareness Cognitive impairment 939001 R42 Dizziness and giddiness Mal De Debarquement syndrome 628001 R47.01 Aphasia 1020001 R53.82 Chronic fatigue, unspecified chronic fatigue syndrome 67001 R62 Lack of expected normal physiological development in childhood and adults Failure To Thrive 56001 R62.50 Unspecified lack of expected normal physiological development in childhood 262001 R62.50 Unspecified lack of expected normal physiological development in childhood Deafness 497001 R62.52 Short stature [child] 1045001 R80 Proteinuria 959001 S06.2 Diffuse traumatic brain injury 570001 T78.40 Allergy, unspecified 1101001 U09.9 Post COVID-19 condition, unspecified Post COVID Tinnitus 1108001 U09.9 Post COVID-19 condition, unspecified Post COVID Tinnitus 770001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Myelodysplastic syndrome, unaffected family member 499001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Shwachman Diamond Syndrome, unaffected family member 252001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Diamond Blackfan Amemia, unaffected family member 276001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Diamond Blackfan Amemia, unaffected family member 298001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Fanconi Anemia, unaffected family member 368001 Z00.6 Encounter for examination for normal comparison and control in clinical research program IBMFS, unaffected family member 667001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Thrombocytopenia Absent Radius, unaffected family member 160001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Trichothiodystrophy, unaffected family member 617001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Holoprosencephaly, unaffected family member 237001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Coloboma of iris, unaffected family member 81001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Enlarged Vestibular Aqueduct [EVA], unaffected family member 964001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Osteogenesis imperfecta, unaffected family member 552001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Xeroderma pigmentosum, unaffected family member 278001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Dyskeratosis Congenita, unaffected family member 233001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Cockayne syndrome, unaffected family member 623001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Bardet-Biedl Syndrome, unaffected family member 505001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Smith-Magenis Syndrome, unaffected family member 604001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Smith-Magenis Syndrome, unaffected family member 1002001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Breacher study 779001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Audiovestibular Healthy Volunteer 772001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Breacher Study 791001 Z00.6 Encounter for examination for normal comparison and control in clinical research program ClinSeq protocol 335001 Z00.6 Encounter for examination for normal comparison and control in clinical research program 804001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Dystonia TMS Study 813001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Epilepsy study 800001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Language delay study 113001 Z00.6 Encounter for examination for normal comparison and control in clinical research program 606001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Sleep Study 963001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Sleep Study 158001 Z00.6 Encounter for examination for normal comparison and control in clinical research program TMS Safety 1000001 Z00.6 Encounter for examination for normal comparison and control in clinical research program Breacher Study 1063001 Z00.6 Encounter for examination for normal comparison and control in clinical research program SEG protocol - Control 282001 Z13.29 Encounter forÊscreeningÊfor other suspectedÊendocrineÊdisorder 305001 Z13.79 Encounter for other screening for genetic and chromosomal anomalies 640001 Z15 Genetic susceptibility to disease Li-Fraumeni Syndrome, Family History 1086001 Z15.09 Genetic susceptibility to other malignant neoplasm CHD1 mutation 1091001 Z15.89 Genetic susceptibility to other disease Germline Runx1 Mutation 192001 Z20.810 Contact with and (suspected) exposure to anthrax 264001 Z82.2 Family history of deafness and hearing loss Autosomal dominant nonsyndromic, DFNA, family 337001 Z82.2 Family history of deafness and hearing loss Family 209001 Z94.81 Bone marrow transplant status 968001 Amikacin 972001 Amikacin2 974001 Amikacin3 677001 Undiagnosed diseases protocol 1065001 Jen study 837001 Crolibulin+Cisplatin 1039001 SEG protocol - AHI 608001 Unknown diagnosis genetic syndrome