Disease Name Symbol Acronym
Aapoai Amyloidosis APM002
Aapoaii Amyloidosis APM001
Aapoaiv Amyloidosis APV001
Aarskog Syndrome, Autosomal Dominant ARS003
Aarskog-Scott Syndrome ARS001
Aase-Smith Syndrome I ASS004
Abacavir Allergy ABC021
Abacavir Toxicity ABC017
Abcd Syndrome ABC001
Abderhalden Kaufmann Lignac Syndrome ABD005
Abdominal Chemodectomas with Cutaneous Angiolipomas ABD006
Abdominal Cystic Lymphangioma ABD007
Abdominal Obesity-Metabolic Syndrome 1 ABD014
Abdominal Obesity-Metabolic Syndrome 3 ABD013
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 ABD017
Abdominal Tuberculosis ABD004
Abdominal Wall Defect ABD010
Abducens Nerve Disease ABD002
Abducens Nerve Neoplasm ABD001
Abducens Palsy ABD009
Aberrant Subclavian Artery ABR001
Abetalipoproteinemia ABT001
Abidi X-Linked Mental Retardation Syndrome ABD008
Ablepharon-Macrostomia Syndrome ABL002
Abnormal Number of Coronary Ostia ABN010
Abnormal Pupillary Function ABN004
Abnormal Retinal Correspondence ABN001
Abnormal Threshold of Rods ABN003
Abnormality of Glucagon Secretion ABN002
Abruzzo-Erickson Syndrome ABR009
Absence of Fingerprints Congenital Milia ABS001
Absence of Innominate Vein ABS017
Absence of Septum Pellucidum ABS003
Absence of the Pulmonary Artery ABS016
Absence of Tibia with Polydactyly ABS005
Absent Breasts and Nipples ABS006
Absent Eyebrows and Eyelashes with Mental Retardation ABS020
Absent Patella ABS007
Acalculous Cholecystitis ACL001
Acalvaria ACL002
Acanthamoeba Keratitis ACN019
Acanthocephaliasis ACN005
Acanthocheilonemiasis ACN013
Acantholytic Acanthoma ACN004
Acantholytic Squamous Cell Skin Carcinoma ACN008
Acantholytic Variant Squamous Cell Breast Carcinoma ACN009
Acanthoma ACN010
Acanthosis Nigricans ACN002
Acanthosis Nigricans with Muscle Cramps and Acral Enlargement ACN028
Acardia ACR022
Acatalasemia ACT209
Accelerated Tumor Formation ACC008
Accessory Mitral Valve Tissue ACC011
Accessory Nerve Disease ACC001
Accessory Pancreas ACC005
Accessory Tricuspid Valve Tissue ACC010
Accommodative Esotropia ACC003
Accommodative Spasm ACC002
Aceruloplasminemia ACR006
Acetaminophen Metabolism ACT149
Acetophenetidin Sensitivity ACT237
Acetylation, Slow ACT133
Acetyl-Carnitine Deficiency ACT090
Acetyl-Coa Acetyltransferase-2 Deficiency ACT239
Acetyl-Coa Carboxylase Deficiency ACT086
Achalasia ACH005
Achalasia, Familial Esophageal ACH015
Achalasia-Addisonianism-Alacrima Syndrome ACH022
Achalasia-Microcephaly Syndrome ACH039
Achard Syndrome ACH006
Achard Thiers Syndrome ACH016
Acheiria ACH028
Acheiropody ACH001
Achenbach Syndrome ACH007
Achilles Bursitis ACH002
Achondrogenesis ACH011
Achondrogenesis, Type Ia ACH033
Achondrogenesis, Type Ib ACH042
Achondrogenesis, Type Ii ACH041
Achondroplasia ACH004
Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans ACH043
Achoo Syndrome ACH040
Achromatopsia ACH003
Achromatopsia 2 ACH020
Achromatopsia 3 ACH021
Achromatopsia 4 ACH023
Achromatopsia 7 ACH038
Acid Anhydride Respiratory Allergy ACD012
Acid Phosphatase Deficiency ACD011
Acid Sphingomyelinase Deficiency ACD003
Acid-Labile Subunit Deficiency ACD008
Acidophil Adenoma ACD001
Acinar Cell Carcinoma ACN001
Acinar Cell Carcinoma of Pancreas ACN026
Acinar Cell Cystadenocarcinoma ACN007
Acinic Cell Breast Carcinoma ACN006
Acitretin Embryopathy ACT091
Acitretin/etretinate Embryopathy ACT206
Ackerman Syndrome ACK001
Acne Inversa, Familial, 1 ACN018
Acne Inversa, Familial, 2, with or Without Dowling-Degos Disease ACN030
Acne Inversa, Familial, 3 ACN016
Acne, Adult ACN029
Acneiform Dermatitis ACN003
Acoustic Neuroma ACS001
Acquired Agranulocytosis ACQ011
Acquired Amegakaryocytic Thrombocytopenia ACQ041
Acquired Aneurysmal Subarachnoid Hemorrhage ACQ033
Acquired Angioedema ACQ012
Acquired Angioedema Type 1 ACQ035
Acquired Angioedema Type 2 ACQ036
Acquired Angioedema with C1inh Deficiency ACQ052
Acquired Central Diabetes Insipidus ACQ034
Acquired Color Blindness ACQ001
Acquired Cutis Laxa ACQ027
Acquired Cystic Disease-Associated Renal Cell Carcinoma ACQ048
Acquired Gastric Outlet Stenosis ACQ006
Acquired Generalized Lipodystrophy ACQ022
Acquired Hemangioma ACQ004
Acquired Hemophagocytic Lymphohistiocytosis Associated with Malignant Disease ACQ049
Acquired Hemophilia ACQ014
Acquired Hemophilia a ACQ042
Acquired Hyperkeratosis ACQ008
Acquired Immunodeficiency Syndrome ACQ007
Acquired Kinky Hair Syndrome ACQ032
Acquired Metabolic Disease ACQ009
Acquired Methemoglobinemia ACQ047
Acquired Monoclonal Ig Light Chain-Associated Fanconi Syndrome ACQ046
Acquired Night Blindness ACQ002
Acquired Polycythemia ACQ010
Acquired Porencephaly ACQ029
Acquired Prothrombin Deficiency ACQ051
Acquired Pseudoxanthoma Elasticum ACQ026
Acquired Pure Red Cell Aplasia ACQ016
Acquired Purpura Fulminans ACQ039
Acquired Schizencephaly ACQ050
Acquired Tear Duct Stenosis ACQ003
Acquired Thrombocytopenia ACQ005
Acquired Von Willebrand Syndrome ACQ017
Acral Dysostosis Dyserythropoiesis Syndrome ACR023
Acral Dystrophic Epidermolysis Bullosa ACR075
Acral Lentiginous Melanoma ACR014
Acral Persistent Papular Mucinosis ACR080
Acral Self-Healing Collodion Baby ACR078
Acrocallosal Syndrome ACR008
Acrocapitofemoral Dysplasia ACR002
Acrocephalopolydactylous Dysplasia ACR025
Acrocephalopolysyndactyly Type Iii ACR106
Acrocephalopolysyndactyly Type Iv ACR108
Acrocraniofacial Dysostosis ACR101
Acrodermatitis ACR005
Acrodermatitis Chronica Atrophicans ACR097
Acrodermatitis Enteropathica, Zinc-Deficiency Type ACR056
Acrodysostosis ACR013
Acrodysostosis 1 with or Without Hormone Resistance ACR110
Acrodysostosis 2 with or Without Hormone Resistance ACR119
Acrodysostosis with Multiple Hormone Resistance ACR079
Acrodysplasia Scoliosis ACR027
Acrodysplasia with Ossification Abnormalities, Short Stature, and Fibular Hypoplasia ACR117
Acrofacial Dysostosis ACR017
Acrofacial Dysostosis 1, Nager Type ACR058
Acrofacial Dysostosis Preis Type ACR031
Acrofacial Dysostosis Syndrome of Rodriguez ACR104
Acrofacial Dysostosis, Catania Type ACR099
Acrofacial Dysostosis, Cincinnati Type ACR095
Acrofacial Dysostosis, Kennedy-Teebi Type ACR083
Acrofacial Dysostosis, Palagonia Type ACR107
Acrofacial Dysostosis, Patagonia Type ACR100
Acrofrontofacionasal Dysostosis ACR093
Acrofrontofacionasal Dysostosis 1 ACR103
Acrofrontofacionasal Dysostosis 2 ACR105
Acrogeria, Gottron Type ACR034
Acrokeratoderma, Hereditary Papulotranslucent ACR111
Acrokeratosis Verruciformis ACR004
Acroleukopathy, Symmetric ACR112
Acromegaloid Changes, Cutis Verticis Gyrata, and Corneal Leukoma ACR113
Acromegaloid Facial Appearance Syndrome ACR037
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia ACR089
Acromegaloid Hypertrichosis Syndrome ACR039
Acromegaly ACR007
Acromelanosis ACR040
Acromelic Frontonasal Dysostosis ACR041
Acromesomelic Dysplasia ACR016
Acromesomelic Dysplasia Campailla Martinelli Type ACR042
Acromesomelic Dysplasia, Demirhan Type ACR096
Acromesomelic Dysplasia, Hunter-Thompson Type ACR009
Acromesomelic Dysplasia, Maroteaux Type ACR011
Acromial Dimples ACR114
Acromicric Dysplasia ACR043
Acroosteolysis ACR062
Acroosteolysis Dominant Type ACR044
Acropectoral Syndrome ACR019
Acro-Pectoro-Renal Field Defect ACR045
Acropectorovertebral Dysplasia ACR020
Acropectorovertebral Dysplasia F Form ACR046
Acrorenal Syndrome ACR072
Acrorenal Syndrome Recessive ACR048
Acrorenal Syndrome, Autosomal Recessive ACR115
Acrorenal-Mandibular Syndrome ACR102
Acrospiroma ACR049
Acsl4-Related Intellectual Disability ACS002
Actg2-Related Disorders ACT215
Acth Deficiency, Isolated ACT238
Acth-Independent Macronodular Adrenal Hyperplasia ACT092
Acth-Independent Macronodular Adrenal Hyperplasia 2 ACT202
Acth-Secreting Pituitary Adenoma ACT010
Actin-Accumulation Myopathy ACT130
Actinic Cheilitis ACT093
Actinic Keratosis ACT008
Actinic Lichen Planus ACT160
Actinic Prurigo ACT164
Actinobacillosis ACT016
Actinomycosis ACT055
Active Cochlear Meniere's Disease ACT015
Active Cochleovestibular Meniere's Disease ACT013
Active Peptic Ulcer Disease ACT058
Active Vestibular Meniere's Disease ACT014
Actn3 Deficiency ACT240
Acute Ackee Fruit Intoxication ACT170
Acute Adrenal Insufficiency ACT150
Acute Allergic Mucoid Otitis Media ACT063
Acute Allergic Sanguinous Otitis Media ACT025
Acute Allergic Serous Otitis Media ACT002
Acute Annular Outer Retinopathy ACT168
Acute Anterolateral Myocardial Infarction ACT052
Acute Apical Periodontitis ACT046
Acute Articular Rheumatism ACT094
Acute Basophilic Leukemia ACT177
Acute Bilirubin Encephalopathy ACT241
Acute Biphenotypic Leukemia ACT095
Acute Canaliculitis ACT026
Acute Cervicitis ACT066
Acute Chest Syndrome ACT017
Acute Cholangitis ACT036
Acute Cholinergic Dysautonomia ACT096
Acute Closed-Angle Glaucoma ACT028
Acute Conjunctivitis ACT067
Acute Contagious Conjunctivitis ACT011
Acute Cor Pulmonale ACT056
Acute Cystitis ACT068
Acute Dacryoadenitis ACT030
Acute Dacryocystitis ACT037
Acute Diarrhea ACT004
Acute Diffuse Nephritis ACT041
Acute Disseminated Encephalomyelitis ACT049
Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion ACT191
Acute Endometritis ACT069
Acute Endophthalmitis ACT047
Acute Erythroid Leukemia ACT098
Acute Ethmoiditis ACT034
Acute Eustachian Salpingitis ACT045
Acute Female Pelvic Peritonitis ACT054
Acute Flaccid Myelitis ACT231
Acute Frontal Sinusitis ACT035
Acute Generalized Exanthematous Pustulosis ACT167
Acute Gonococcal Cervicitis ACT048
Acute Gonococcal Cystitis ACT006
Acute Gonococcal Endometritis ACT057
Acute Gonococcal Epididymo-Orchitis ACT039
Acute Gonococcal Prostatitis ACT024
Acute Gonococcal Salpingitis ACT023
Acute Graft Versus Host Disease ACT135
Acute Hemorrhagic Conjunctivitis ACT012
Acute Hemorrhagic Encephalitis ACT065
Acute Hemorrhagic Leukoencephalitis ACT032
Acute Hydrops Keratoconus ACT005
Acute Infection of Pinna ACT044
Acute Inferolateral Myocardial Infarction ACT051
Acute Inferoposterior Infarction ACT050
Acute Inflammation of Lacrimal Passage ACT070
Acute Insulin Response ACT088
Acute Interstitial Pneumonia ACT029
Acute Kidney Failure ACT071
Acute Kidney Tubular Necrosis ACT003
Acute Laryngitis ACT072
Acute Laryngopharyngitis ACT018
Acute Leukemia ACT073
Acute Leukemia of Ambiguous Lineage ACT216
Acute Liver Failure ACT134
Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia ACT102
Acute Lymphoblastic Leukemia, Childhood ACT103
Acute Lymphocytic Leukemia ACT074
Acute Macular Neuroretinopathy ACT235
Acute Maxillary Sinusitis ACT059
Acute Megakaryoblastic Leukemia in Down Syndrome ACT186
Acute Megakaryoblastic Leukemia Without Down Syndrome ACT165
Acute Monoblastic Leukemia ACT200
Acute Motor and Sensory Axonal Neuropathy ACT236
Acute Motor Axonal Neuropathy ACT181
Acute Mountain Sickness ACT105
Acute Myeloblastic Leukemia with Maturation ACT113
Acute Myeloblastic Leukemia Without Maturation ACT114
Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent ACT184
Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation ACT158
Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor ACT185
Acute Myeloid Leukemia with 11q23 Abnormalities ACT179
Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) ACT193
Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) ACT196
Acute Myeloid Leukemia with Minimal Differentiation ACT234
Acute Myeloid Leukemia with Npm1 Somatic Mutations ACT199
Acute Myeloid Leukemia with Recurrent Genetic Anomaly ACT217
Acute Myeloid Leukemia with T(6;9)(p23;q34) ACT198
Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation ACT190
Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation ACT194
Acute Myeloid Leukemia with T(9;11)(p22;q23) ACT195
Acute Myocardial Infarction ACT075
Acute Myocarditis ACT076
Acute Necrotizing Encephalitis ACT064
Acute Necrotizing Encephalopathy ACT232
Acute Necrotizing Encephalopathy Type 1 ACT229
Acute Neonatal Citrullinemia Type I ACT189
Acute Non Lymphoblastic Leukemia ACT118
Acute Opioid Poisoning ACT171
Acute Orbital Inflammation ACT077
Acute Pancreatitis ACT027
Acute Pandysautonomia ACT161
Acute Panmyelosis with Myelofibrosis ACT176
Acute Pericementitis ACT062
Acute Perichondritis of Pinna ACT007
Acute Peripheral Arterial Occlusion ACT174
Acute Poisoning by Drugs with Membrane-Stabilizing Effect ACT173
Acute Porphyria ACT078
Acute Posterior Multifocal Placoid Pigment Epitheliopathy ACT201
Acute Poststreptococcal Glomerulonephritis ACT040
Acute Proliferative Glomerulonephritis ACT079
Acute Promyelocytic Leukemia ACT119
Acute Pulmonary Heart Disease ACT080
Acute Pure Sensory Neuropathy ACT163
Acute Pyelonephritis ACT042
Acute Radiation Syndrome ACT228
Acute Respiratory Coronavirus Infection ACT227
Acute Respiratory Distress Syndrome ACT210
Acute Retinal Necrosis Syndrome ACT022
Acute Retrobulbar Neuritis ACT038
Acute Salpingitis ACT081
Acute Salpingo-Oophoritis ACT031
Acute Sanguinous Otitis Media ACT082
Acute Sensory Ataxic Neuropathy ACT162
Acute Serous Otitis Media ACT083
Acute Sphenoidal Sinusitis ACT061
Acute Stress Disorder ACT084
Acute T Cell Leukemia ACT020
Acute Thyroiditis ACT053
Acute Transverse Myelitis ACT159
Acute Tricyclic Antidepressant Poisoning ACT172
Acute Tympanitis ACT001
Acute Urate Nephropathy ACT043
Acute Vascular Insufficiency of Intestine ACT060
Acute Zonal Occult Outer Retinopathy ACT120
Acylase, Cobalt-Activated ACY008
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of ACY009
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of ACY005
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of ACY010
Adactylia, Unilateral ADC008
Adamantinoid Basal Cell Epithelioma ADM002
Adamantinoma of Long Bones ADM013
Adamantinous Craniopharyngioma ADM001
Adams-Oliver Syndrome ADM011
Adams-Oliver Syndrome 1 ADM005
Adams-Oliver Syndrome 2 ADM007
Adams-Oliver Syndrome 3 ADM008
Adams-Oliver Syndrome 4 ADM009
Adams-Oliver Syndrome 5 ADM010
Adams-Oliver Syndrome 6 ADM012
Adamtsl4-Related Eye Disorders ADM003
Adcy5-Related Dyskinesia ADC005
Adducted Thumbs Syndrome ADD006
Adenine Phosphoribosyltransferase Deficiency ADN024
Adenocarcinoid Tumor ADN026
Adenocarcinoma ADN016
Adenocarcinoma in Situ ADN012
Adenocarcinoma of the Gallbladder and Extrahepatic Biliary Tract ADN082
Adenocarcinoma of the Liver and Intrahepatic Biliary Tract ADN087
Adenocarcinoma of the Penis ADN086
Adenofibroma ADN017
Adenohypophysitis ADN064
Adenoid Basal Carcinoma of the Cervix Uteri ADN062
Adenoid Basal Cell Carcinoma ADN015
Adenoid Cystic Carcinoma ADN011
Adenoid Cystic Carcinoma of the Corpus Uteri ADN060
Adenoid Hypertrophy ADN067
Adenoid Squamous Cell Carcinoma ADN013
Adenoiditis ADN002
Adenoma ADN018
Adenoma of Pancreas ADN072
Adenomatoid Tumor ADN014
Adenomyoma ADN075
Adenomyoma of Uterine Corpus ADN019
Adenomyosis ADN027
Adenosarcoma ADN020
Adenosarcoma of the Cervix Uteri ADN061
Adenosarcoma of the Corpus Uteri ADN059
Adenosarcoma of the Uterus ADN028
Adenosine Deaminase Deficiency ADN001
Adenosine Deaminase, Elevated, Hemolytic Anemia Due to ADN084
Adenosine Monophosphate Deaminase 1 Deficiency ADN029
Adenosine Triphosphatase Deficiency, Anemia Due to ADN079
Adenosine Triphosphate, Elevated, of Erythrocytes ADN039
Adenosquamous Bile Duct Carcinoma ADN003
Adenosquamous Breast Carcinoma ADN004
Adenosquamous Carcinoma ADN009
Adenosquamous Colon Carcinoma ADN006
Adenosquamous Gallbladder Carcinoma ADN005
Adenosquamous Lung Carcinoma ADN089
Adenosquamous Prostate Carcinoma ADN007
Adenovirus Infection in Immunocompromised Patients ADN063
Adenylate Kinase Deficiency, Hemolytic Anemia Due to ADN085
Adenylosuccinase Deficiency ADN022
Adenylosuccinase Lyase Deficiency ADN058
Adermatoglyphia ADR038
Adhesions of Uterus ADH001
Adhesive Otitis Media ADH006
Adiaspiromycosis ADS001
Adie Pupil ADP007
Adiponectin, Serum Level of, Quantitative Trait Locus 1 ADP010
Adiponectin, Serum Level of, Quantitative Trait Locus 2 ADP008
Adiponectin, Serum Level of, Quantitative Trait Locus 3 ADP009
Adiponectin, Serum Level of, Quantitative Trait Locus 4 ADP011
Adiponectin, Serum Level of, Quantitative Trait Locus 5 ADP012
Adiposis Dolorosa ADP001
Adjustment Disorder ADJ001
Adnexal Spiradenoma/cylindroma of a Sweat Gland ADN030
Adnp Syndrome ADN078
Adnp-Related Intellectual Disability and Autism Spectrum Disorder ADN076
Adolescence-Adult Electroclinical Syndrome ADL051
Adrenal Adenoma ADR008
Adrenal Carcinoma ADR005
Adrenal Cortex Disease ADR009
Adrenal Cortical Adenocarcinoma ADR004
Adrenal Cortical Adenoma ADR041
Adrenal Cortical Carcinoma ADR016
Adrenal Cortical Hypofunction ADR010
Adrenal Gland Disease ADR012
Adrenal Gland Ganglioneuroblastoma ADR006
Adrenal Gland Pheochromocytoma ADR040
Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency ADR052
Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency ADR042
Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency ADR048
Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency ADR051
Adrenal Hypoplasia, Congenital ADR049
Adrenal Hypoplasia, Congenital, with Absent Pituitary Luteinizing Hormone ADR047
Adrenal Hypoplasia, Cytomegalic Type ADR053
Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete ADR056
Adrenal Medulla Cancer ADR014
Adrenal Neuroblastoma ADR003
Adrenal Rest Tumor ADR001
Adrenocortical Carcinoma with Pure Aldosterone Hypersecretion ADR035
Adrenocortical Carcinoma, Hereditary ADR054
Adrenocortical Hypofunction, Chronic Primary Congenital ADR050
Adrenocortical Unresponsiveness to Acth with Postreceptor Defect ADR055
Adrenoleukodystrophy ADR007
Adrenomyeloneuropathy ADR022
Adrenomyodystrophy ADR023
Adult Acute Lymphocytic Leukemia ADL052
Adult Acute Monocytic Leukemia ADL093
Adult Acute Respiratory Distress Syndrome ADL080
Adult Astrocytic Tumour ADL053
Adult Botryoid Rhabdomyosarcoma ADL031
Adult Brain Ependymoma ADL040
Adult Brain Stem Glioma ADL054
Adult Brainstem Astrocytoma ADL004
Adult Brainstem Gliosarcoma ADL021
Adult Brainstem Mixed Glioma ADL003
Adult Central Nervous System Choriocarcinoma ADL024
Adult Central Nervous System Embryonal Carcinoma ADL007
Adult Central Nervous System Germinoma ADL036
Adult Central Nervous System Immature Teratoma ADL012
Adult Central Nervous System Mature Teratoma ADL011
Adult Central Nervous System Mixed Germ Cell Tumor ADL029
Adult Central Nervous System Primitive Neuroectodermal Neoplasm ADL022
Adult Central Nervous System Teratoma ADL055
Adult Cerebellar Neoplasm ADL026
Adult Choroid Plexus Cancer ADL018
Adult Cystic Teratoma ADL013
Adult Dermatomyositis ADL027
Adult Endodermal Sinus Tumor ADL047
Adult Ependymoblastoma ADL045
Adult Epithelioid Sarcoma ADL038
Adult Extraosseous Chondrosarcoma ADL028
Adult Extraosseous Osteosarcoma ADL034
Adult Familial Nephronophthisis-Spastic Quadriparesia Syndrome ADL092
Adult Fibrosarcoma ADL019
Adult Hepatocellular Carcinoma ADL096
Adult Infiltrating Astrocytic Neoplasm ADL044
Adult Intestinal Botulism ADL069
Adult Intracranial Malignant Hemangiopericytoma ADL049
Adult Krabbe Disease ADL071
Adult Leptomeningeal Melanoma ADL009
Adult Liposarcoma ADL015
Adult Lymphoma ADL001
Adult Malignant Hemangiopericytoma ADL048
Adult Malignant Mesenchymoma ADL020
Adult Malignant Schwannoma ADL042
Adult Medulloblastoma ADL023
Adult Mesenchymal Chondrosarcoma ADL005
Adult Mesoblastic Nephroma ADL014
Adult Myxoid Chondrosarcoma ADL046
Adult Neuronal Ceroid Lipofuscinosis ADL066
Adult Oligodendroglioma ADL008
Adult Papillary Meningioma ADL033
Adult Pineal Parenchymal Tumor ADL056
Adult Pineoblastoma ADL025
Adult Polyglucosan Body Disease ADL060
Adult Progressive Spinal Muscular Atrophy Aran Duchenne Type ADL062
Adult Pulmonary Langerhans Cell Histiocytosis ADL082
Adult Respiratory Distress Syndrome ADL010
Adult Spinal Cord Ependymoma ADL041
Adult Spinal Cord Glioblastoma Multiforme ADL035
Adult Syndrome ADL002
Adult T-Cell Leukemia ADL017
Adult Teratoma ADL057
Adult Type Testicular Granulosa Cell Tumor ADL043
Adult Vagina Botryoid Rhabdomyosarcoma ADL032
Adult Xanthogranuloma ADL037
Adult-Onset Citrullinemia Type I ADL083
Adult-Onset Distal Myopathy Due to Vcp Mutation ADL074
Adult-Onset Immunodeficiency with Anti-Interferon-Gamma Autoantibodies ADL095
Adult-Onset Myasthenia Gravis ADL084
Adult-Onset Nemaline Myopathy ADL068
Adult-Onset Non-Insulinoma Persistent Hyperinsulinemic Hypoglycemia ADL070
Adult-Onset Still's Disease ADL030
Advanced Sleep Phase Syndrome ADV001
Advanced Sleep Phase Syndrome 2 ADV008
Advanced Sleep Phase Syndrome, Familial, 1 ADV003
Advanced Sleep Phase Syndrome, Familial, 2 ADV007
Advanced Sleep Phase Syndrome, Familial, 3 ADV006
Adverse Events of 5-Alpha-Reductase Inhibitors ADV004
Aerobic Actinomyces Infection ARB002
Afferent Loop Syndrome AFF001
Afib Amyloidosis AFB003
Afibrinogenemia AFB001
Afibrinogenemia, Congenital AFB002
Aflatoxins-Related Hepatocellular Carcinoma AFL001
African Histoplasmosis AFR001
African Tick-Bite Fever AFR002
Agammaglobulinemia AGM001
Agammaglobulinemia 1, Autosomal Recessive AGM013
Agammaglobulinemia 2, Autosomal Recessive AGM021
Agammaglobulinemia 3, Autosomal Recessive AGM022
Agammaglobulinemia 4, Autosomal Recessive AGM023
Agammaglobulinemia 5, Autosomal Dominant AGM024
Agammaglobulinemia 6, Autosomal Recessive AGM020
Agammaglobulinemia 7, Autosomal Recessive AGM015
Agammaglobulinemia 8, Autosomal Dominant AGM017
Agammaglobulinemia, Microcephaly, and Severe Dermatitis AGM003
Agammaglobulinemia, Non-Bruton Type AGM004
Agammaglobulinemia, X-Linked AGM019
Aganglionosis, Total Intestinal AGN004
Agenesis and Aplasia of Uterine Body AGN009
Agenesis of Cerebral White Matter AGN015
Agenesis of the Corpus Callosum and Congenital Lymphedema AGN017
Agenesis of the Corpus Callosum with Peripheral Neuropathy AGN003
Agenesis of the Superior Vena Cava AGN011
Age-Related Hearing Impairment 1 AGR013
Age-Related Hearing Impairment 2 AGR014
Age-Related Hearing Loss AGR019
Aggressive Digital Papillary Adenocarcinoma AGG003
Aggressive Periodontitis AGG001
Aggressive Systemic Mastocytosis AGG002
Aging AGN016
Aglossia and Situs Inversus AGL001
Agnathia-Microstomia-Synotia AGN006
Agnathia-Otocephaly Complex AGN012
Agnosia AGN002
Agoraphobia AGR002
Agraphia AGR018
Agyria Pachygyria Polymicrogyria AGY001
Agyria-Pachygyria Type 1 AGY002
Ah Amyloidosis AHM002
Ahumada Del Castillo Syndrome AHM001
Aicar Transformylase/imp Cyclohydrolase Deficiency ACR118
Aicardi Syndrome ACR012
Aicardi-Goutieres Syndrome ACR001
Aicardi-Goutieres Syndrome 1 ACR116
Aicardi-Goutieres Syndrome 2 ACR090
Aicardi-Goutieres Syndrome 3 ACR088
Aicardi-Goutieres Syndrome 4 ACR091
Aicardi-Goutieres Syndrome 5 ACR092
Aicardi-Goutieres Syndrome 6 ACR081
Aicardi-Goutieres Syndrome 7 ACR084
Aids - Neurological Complications ADS006
Aids Dementia Complex ADS004
Aids Dysmorphic Syndrome ADS005
Aids Phobia ADS003
Aids Wasting Syndrome ADS015
Ainhum ANH001
Aip-Related Familial Isolated Pituitary Adenomas APR002
Airway-Centered Interstitial Fibrosis ARW003
Akaba Hayasaka Syndrome AKB001
Akesson Syndrome AKS001
Akinetic Mutism AKN002
Akinetopsia AKN001
Aksu Von Stockhausen Syndrome AKS002
Al Amyloidosis ALM001
Al Gazali Aziz Salem Syndrome ALG003
Al Gazali Khidr Prem Chandran Syndrome ALG004
Al Gazali Sabrinathan Nair Syndrome ALG005
Al Kaissi Syndrome ALK023
Alacrima, Achalasia, and Mental Retardation Syndrome ALC028
Alacrima, Congenital, Autosomal Dominant ALC031
Alacrima, Congenital, Autosomal Recessive ALC032
Alagille Syndrome 1 ALG028
Alagille Syndrome 2 ALG016
Aland Island Eye Disease ALN001
Alanine Aminotransferase, Plasma Level of, Quantitative Trait Locus 1 ALN004
Alanine Aminotransferase, Plasma Level of, Quantitative Trait Locus 2 ALN005
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus ALN003
Alar Cleft, Isolated ALR004
Alazami Syndrome ALZ030
Alazami-Yuan Syndrome ALZ044
Albinism ALB002
Albinism, Minimal Pigment Type ALB006
Albinism, Ocular, Type I ALB024
Albinism, Ocular, with Late-Onset Sensorineural Deafness ALB025
Albinism, Ocular, with Sensorineural Deafness ALB023
Albinism, Oculocutaneous, Type Ia ALB009
Albinism, Oculocutaneous, Type Ib ALB010
Albinism, Oculocutaneous, Type Ii ALB021
Albinism, Oculocutaneous, Type Iii ALB020
Albinism, Oculocutaneous, Type Iv ALB019
Albinism, Oculocutaneous, Type V ALB015
Albinism, Oculocutaneous, Type Vi ALB017
Albinism, Oculocutaneous, Type Vii ALB016
Albinism-Deafness Syndrome ALB003
Albinism-Microcephaly-Digital Anomalies Syndrome ALB022
Albright Like Syndrome ALB007
Albright's Hereditary Osteodystrophy ALB001
Alcohol Abuse ALC004
Alcohol Dependence ALC007
Alcohol Sensitivity, Acute ALC016
Alcoholic Cardiomyopathy ALC010
Alcoholic Gastritis ALC012
Alcoholic Hepatitis ALC006
Alcoholic Liver Cirrhosis ALC009
Alcoholic Neuropathy ALC011
Alcoholic Pancreatitis ALC005
Alcoholic Psychosis ALC003
Alcohol-Induced Mental Disorder ALC013
Alcohol-Related Birth Defect ALC001
Alcohol-Related Neurodevelopmental Disorder ALC002
Alcuronium Bromide Allergy ALC034
Aldosterone-Producing Adenoma ALD013
Aldred Syndrome ALD006
Alect2 Amyloidosis ALC030
Aleukemic Leukemia Cutis ALK003
Aleukemic Mast Cell Leukemia ALK014
Aleukemic Monocytic Leukemia Cutis ALK002
Aleutian Mink Disease ALT002
Alexander Disease ALX003
Alexia ALX001
Alexithymia ALX002
Alezzandrini Syndrome ALZ038
Alg12-Congenital Disorder of Glycosylation ALG019
Alg1-Congenital Disorder of Glycosylation ALG025
Alg6-Congenital Disorder of Glycosylation ALG024
Al-Gazali Syndrome ALG026
Al-Gazali-Bakalinova Syndrome ALG027
Al-Gazali-Donnai-Mueller Syndrome ALG007
Algoneurodystrophy ALG001
Alien Hand Syndrome ALN006
Alk+ Histiocytosis ALK005
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 ALK019
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 2 ALK020
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 3 ALK021
Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 4 ALK022
Alkaptonuria ALK013
Alkhurma Hemorrhagic Fever ALK001
Alk-Negative Anaplastic Large Cell Lymphoma ALK016
Alk-Positive Anaplastic Large Cell Lymphoma ALK015
Alk-Positive Large B-Cell Lymphoma ALK017
Alk-Related Neuroblastic Tumor Susceptibility ALK018
Alkuraya-Kucinskas Syndrome ALK024
Allain-Babin-Demarquez Syndrome ALL011
Allan-Herndon-Dudley Syndrome ALL001
Allergic Angiitis ALL012
Allergic Asthma ALL006
Allergic Bronchopulmonary Aspergillosis ALL008
Allergic Bronchopulmonary Aspergillosis, Familial ALL027
Allergic Conjunctivitis ALL009
Allergic Contact Dermatitis ALL010
Allergic Contact Dermatitis of Eyelid ALL005
Allergic Cutaneous Vasculitis ALL002
Allergic Encephalomyelitis ALL014
Allergic Hypersensitivity Disease ALL026
Allergic Rhinitis ALL003
Allergic Urticaria ALL007
Allescheriosis ALL004
Allopurinol Toxicity ALL025
Alobar Holoprosencephaly ALB014
Alopecia ALP008
Alopecia Antibody Deficiency ALP049
Alopecia Areata ALP009
Alopecia Areata 1 ALP039
Alopecia Areata 2 ALP040
Alopecia Intellectual Disability Syndrome 2 ALP081
Alopecia Totalis ALP048
Alopecia Universalis Congenita ALP097
Alopecia Universalis Congenita, Xy Gonadal Dysgenesis, and Laryngomalacia ALP102
Alopecia Universalis Onychodystrophy Vitiligo ALP024
Alopecia, Androgenetic, 1 ALP061
Alopecia, Androgenetic, 2 ALP036
Alopecia, Androgenetic, 3 ALP037
Alopecia, Congenital ALP099
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality ALP025
Alopecia, Familial Focal ALP096
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome ALP041
Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality ALP089
Alopecia-Contractures-Dwarfism Mental Retardation Syndrome ALP091
Alopecia-Contractures-Dwarfism-Intellectual Disability Syndrome ALP067
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan ALP092
Alopecia-Intellectual Disability Syndrome ALP068
Alopecia-Mental Retardation Syndrome 1 ALP076
Alopecia-Mental Retardation Syndrome 2 ALP075
Alopecia-Mental Retardation Syndrome 3 ALP063
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism ALP090
Alpha Chain Disease ALP005
Alpha Thalassemia-Intellectual Disability Syndrome Type 1 ALP094
Alpha Thalassemia-X-Linked Intellectual Disability Syndrome ALP095
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity ALP042
Alpha-1-Antitrypsin Deficiency ALP103
Alpha-2-Deficient Collagen Disease ALP098
Alpha-2-Macroglobulin Deficiency ALP062
Alpha-2-Plasmin Inhibitor Deficiency ALP043
Alpha-Fetoprotein Deficiency ALP072
Alpha-Fetoprotein, Hereditary Persistence of ALP088
Alpha-Heavy Chain Disease ALP087
Alpha-Ketoglutarate Dehydrogenase Deficiency ALP011
Alpha-Mannosidosis, Adult Form ALP056
Alpha-Mannosidosis, Infantile Form ALP055
Alpha-Methylacetoacetic Aciduria ALP077
Alpha-Methylacyl-Coa Racemase Deficiency ALP012
Alpha-Thalassemia ALP101
Alpha-Thalassemia Myelodysplasia Syndrome ALP013
Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related ALP093
Alpha-Thalassemia/mental Retardation Syndrome, X-Linked ALP100
Alpha-Thalassemia-Abnormal Morphogenesis ALP029
Alport Syndrome ALP004
Alport Syndrome 1, X-Linked ALP106
Alport Syndrome 2, Autosomal Recessive ALP105
Alport Syndrome 3, Autosomal Dominant ALP104
Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome ALP085
Al-Raqad Syndrome ALR002
Als2-Related Disorders ALS003
Alsing Syndrome ALS004
Alstrom Syndrome ALS001
Alternating Esotropia ALT004
Alternating Exotropia ALT003
Alternating Hemiplegia of Childhood ALT001
Alternating Hemiplegia of Childhood 1 ALT008
Alternating Hemiplegia of Childhood 2 ALT007
Aluminosis ALM003
Alveolar Capillary Dysplasia ALV006
Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins ALV007
Alveolar Echinococcosis ALV002
Alveolar Periostitis ALV001
Alveolar Soft Part Sarcoma ALV005
Alveoli Adenoma ALV003
Alzheimer Disease ALZ034
Alzheimer Disease 10 ALZ057
Alzheimer Disease 11 ALZ058
Alzheimer Disease 12 ALZ012
Alzheimer Disease 13 ALZ059
Alzheimer Disease 14 ALZ060
Alzheimer Disease 15 ALZ061
Alzheimer Disease 16 ALZ014
Alzheimer Disease 17 ALZ031
Alzheimer Disease 18 ALZ032
Alzheimer Disease 19 ALZ062
Alzheimer Disease 2 ALZ049
Alzheimer Disease 3 ALZ056
Alzheimer Disease 4 ALZ054
Alzheimer Disease 5 ALZ050
Alzheimer Disease 6 ALZ015
Alzheimer Disease 7 ALZ053
Alzheimer Disease 8 ALZ016
Alzheimer Disease 9 ALZ045
Alzheimer Disease Mitochondrial ALZ029
Alzheimer Disease Without Neurofibrillary Tangles ALZ051
Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology ALZ052
Alzheimer's Disease 1 ALZ063
Amastia, Bilateral, with Ureteral Triplication and Dysmorphism AMS004
Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis AMR007
Amaurosis Fugax AMR003
Amblyopia AMB002
Amebiasis AMB001
Amegakaryocytic Thrombocytopenia, Congenital AMG001
Amelanotic Melanoma AML001
Amelia and Terminal Transverse Hemimelia AML060
Amelia of Lower Limb AML036
Amelia of Upper Limb AML037
Amelia, Autosomal Recessive AML053
Ameloblastic Carcinoma AML004
Ameloblastoma AML029
Amelogenesis Imperfecta AML002
Amelogenesis Imperfecta Hypomaturation Type AML005
Amelogenesis Imperfecta Hypoplastic Type, Ig AML006
Amelogenesis Imperfecta Local Hypoplastic AML008
Amelogenesis Imperfecta Pigmented Hypomaturation Type AML010
Amelogenesis Imperfecta Type 2a1 AML063
Amelogenesis Imperfecta, Hypomaturation Type, Iia1 AML013
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 AML014
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 AML015
Amelogenesis Imperfecta, Hypomaturation Type, Iia4 AML039
Amelogenesis Imperfecta, Hypomaturation Type, Iia5 AML062
Amelogenesis Imperfecta, Hypomaturation Type, Iia6 AML058
Amelogenesis Imperfecta, Hypoplastic/hypomaturation, X-Linked 2 AML011
Amelogenesis Imperfecta, Type Ia AML047
Amelogenesis Imperfecta, Type Ib AML017
Amelogenesis Imperfecta, Type Ic AML018
Amelogenesis Imperfecta, Type Ie AML061
Amelogenesis Imperfecta, Type if AML050
Amelogenesis Imperfecta, Type Ig AML044
Amelogenesis Imperfecta, Type Ih AML048
Amelogenesis Imperfecta, Type Iiia AML057
Amelogenesis Imperfecta, Type Iiib AML056
Amelogenesis Imperfecta, Type Iiic AML064
Amelogenesis Imperfecta, Type Ij AML059
Amelogenesis Imperfecta, Type Iv AML020
Ameloonychohypohidrotic Syndrome AML012
Amenorrhea AMN001
Amenorrhea-Galactorrhea Syndrome AMN015
American Histoplasmosis AMR001
Ametropic Amblyopia AMT001
Amino Acid Metabolic Disorder AMN002
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis AMN016
Aminoacidopathies AMN012
Aminoaciduria AMN006
Aminoacylase 1 Deficiency AMN007
Aminolevulinate Dehydratase Deficiency Porphyria AMN008
Aminolevulinic Acid Dehydratase Deficiency Porphyria AMN017
Aminopterin Syndrome Sine Aminopterin AMN014
Aminopterin/methotrexate Embryofetopathy AMN013
Aml with Myelodysplasia-Related Features AML051
Amme Complex AMM001
Amnestic Disorder AMN003
Amniotic Band Syndrome AMN009
Amobarbital, Deficient N-Hydroxylation of AMB006
Amodiaquine Allergy AMD001
Amoebiasis Due to Free-Living Amoebae AMB005
Amoxicillin Allergy AMX001
Amphetamine Abuse AMP007
Ampola Syndrome AMP011
Ampulla of Vater Adenocarcinoma AMP009
Ampulla of Vater Adenosquamous Carcinoma AMP004
Ampulla of Vater Cancer AMP013
Ampulla of Vater Clear Cell Adenocarcinoma AMP008
Ampulla of Vater Mucinous Adenocarcinoma AMP001
Ampulla of Vater Neoplasm AMP003
Ampulla of Vater Small Cell Carcinoma AMP002
Ampulla of Vater Squamous Cell Carcinoma AMP006
Ampullary Signet Ring Cell Adenocarcinoma AMP005
Amusia AMS001
Amyloid Neuropathy AMY005
Amyloid Tumor AMY002
Amyloidosis AMY004
Amyloidosis Aa AMY009
Amyloidosis Beta2m AMY010
Amyloidosis Bronchopulmonary AMY011
Amyloidosis Nodular Localized Cutaneous AMY014
Amyloidosis of Gingiva and Conjunctiva with Intellectual Disability AMY096
Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation AMY015
Amyloidosis, Cutaneous Bullous AMY101
Amyloidosis, Familial Visceral AMY082
Amyloidosis, Finnish Type AMY084
Amyloidosis, Hereditary, Transthyretin-Related AMY087
Amyloidosis, Primary Localized Cutaneous, 1 AMY060
Amyloidosis, Primary Localized Cutaneous, 2 AMY056
Amyloidosis, Primary Localized Cutaneous, 3 AMY111
Amyotonia Congenita AMY018
Amyotrophic Dystonic Paraplegia AMY100
Amyotrophic Lateral Sclerosis 1 AMY091
Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia AMY106
Amyotrophic Lateral Sclerosis 11 AMY083
Amyotrophic Lateral Sclerosis 12 AMY062
Amyotrophic Lateral Sclerosis 14 with or Without Frontotemporal Dementia AMY107
Amyotrophic Lateral Sclerosis 15 with or Without Frontotemporal Dementia AMY104
Amyotrophic Lateral Sclerosis 16, Juvenile AMY057
Amyotrophic Lateral Sclerosis 17 AMY055
Amyotrophic Lateral Sclerosis 18 AMY067
Amyotrophic Lateral Sclerosis 19 AMY059
Amyotrophic Lateral Sclerosis 2, Juvenile AMY058
Amyotrophic Lateral Sclerosis 20 AMY063
Amyotrophic Lateral Sclerosis 21 AMY069
Amyotrophic Lateral Sclerosis 22 with or Without Frontotemporal Dementia AMY099
Amyotrophic Lateral Sclerosis 23 AMY108
Amyotrophic Lateral Sclerosis 24 AMY110
Amyotrophic Lateral Sclerosis 25 AMY112
Amyotrophic Lateral Sclerosis 3 AMY088
Amyotrophic Lateral Sclerosis 4, Juvenile AMY045
Amyotrophic Lateral Sclerosis 5, Juvenile AMY094
Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia AMY105
Amyotrophic Lateral Sclerosis 7 AMY089
Amyotrophic Lateral Sclerosis 8 AMY090
Amyotrophic Lateral Sclerosis 9 AMY085
Amyotrophic Lateral Sclerosis Type 14 AMY074
Amyotrophic Lateral Sclerosis Type 15 AMY079
Amyotrophic Lateral Sclerosis Type 22 AMY109
Amyotrophic Lateral Sclerosis Type 5 AMY022
Amyotrophic Lateral Sclerosis Type 6 AMY023
Amyotrophic Lateral Sclerosis with Polyglucosan Bodies AMY103
Amyotrophic Lateral Sclerosis, Juvenile, with Dementia AMY102
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 AMY027
Amyotrophic Neuralgia AMY003
Amyotrophy, Hereditary Neuralgic AMY086
Amyotrophy, Monomelic AMY098
Anaerobic Meningitis ANR005
Anaerobic Pneumonia ANR006
Anal Atresia, Hypospadias, and Penoscrotal Inversion ANL024
Anal Buschke-Lowenstein Tumor ANL003
Anal Canal Adenocarcinoma ANL014
Anal Canal Carcinoma ANL011
Anal Canal Paget's Disease ANL009
Anal Canal Squamous Cell Carcinoma ANL004
Anal Carcinoma in Situ ANL008
Anal Colloid Adenocarcinoma ANL001
Anal Fistula ANL022
Anal Gland Adenocarcinoma ANL012
Anal Gland Neoplasm ANL002
Anal Margin Basal Cell Carcinoma ANL013
Anal Margin Carcinoma ANL016
Anal Margin Squamous Cell Carcinoma ANL007
Anal Neuroendocrine Tumor ANL010
Anal Paget's Disease ANL006
Anal Spasm ANL005
Anal Sphincter Dysplasia ANL019
Anal Sphincter Myopathy, Internal ANL025
Anal Squamous Cell Carcinoma ANL017
Analbuminemia ANL018
Anaplastic Ependymoma ANP006
Anaplastic Ganglioglioma ANP007
Anaplastic Large Cell Lymphoma ANP001
Anaplastic Oligoastrocytoma ANP008
Anaplastic Oligodendroglioma ANP009
Anaplastic Plasmacytoma ANP010
Anaplastic Pleomorphic Xanthoastrocytoma ANP032
Anaplastic Small Cell Lymphoma ANP011
Anaplastic/large Cell Medulloblastoma ANP028
Anatomical Narrow Angle Borderline Glaucoma ANT015
Anauxetic Dysplasia 1 ANX007
Anauxetic Dysplasia 2 ANX008
Anca-Associated Vasculitis ANC002
Ancylostomiasis ANC001
Andersen Cardiodysrhythmic Periodic Paralysis AND019
Androgen Insensitivity Syndrome AND002
Androgen Insensitivity Syndrome, Mild AND005
Androgen Insensitivity, Partial AND020
Androgenic Alopecia AND014
Androstenone, Ability to Smell AND018
Anemia of Prematurity ANM001
Anemia, Autoimmune Hemolytic ANM038
Anemia, Congenital Dyserythropoietic, Type Ia ANM043
Anemia, Congenital Dyserythropoietic, Type Ib ANM049
Anemia, Congenital Dyserythropoietic, Type Ii ANM042
Anemia, Congenital Dyserythropoietic, Type Iii ANM037
Anemia, Congenital Dyserythropoietic, Type Iv ANM048
Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/mental Retardation Syndrome ANM047
Anemia, Hypochromic Microcytic, with Iron Overload 1 ANM035
Anemia, Hypochromic Microcytic, with Iron Overload 2 ANM027
Anemia, Nonspherocytic Hemolytic, Associated with Abnormality of Red Cell Membrane ANM040
Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency ANM045
Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism ANM041
Anemia, Sideroblastic, 1 ANM036
Anemia, Sideroblastic, 2, Pyridoxine-Refractory ANM033
Anemia, Sideroblastic, 3, Pyridoxine-Refractory ANM032
Anemia, Sideroblastic, 4 ANM034
Anemia, Sideroblastic, and Spinocerebellar Ataxia ANM046
Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive ANM039
Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities ANM044
Anencephaly ANN002
Anencephaly and Spina Bifida X-Linked ANN003
Aneruptive Fever ANR001
Aneurysm of Interventricular Septum ANR045
Aneurysm of Sinus of Valsalva ANR010
Aneurysm or Dilatation of Ascending Aorta ANR037
Aneurysm, Intracranial Berry, 1 ANR027
Aneurysm, Intracranial Berry, 10 ANR025
Aneurysm, Intracranial Berry, 11 ANR039
Aneurysm, Intracranial Berry, 2 ANR011
Aneurysm, Intracranial Berry, 3 ANR028
Aneurysm, Intracranial Berry, 4 ANR022
Aneurysm, Intracranial Berry, 5 ANR026
Aneurysm, Intracranial Berry, 6 ANR029
Aneurysm, Intracranial Berry, 7 ANR023
Aneurysm, Intracranial Berry, 8 ANR030
Aneurysm, Intracranial Berry, 9 ANR024
Aneurysmal Bone Cysts ANR009
Angelman Syndrome ANG001
Angelman Syndrome Due to a Point Mutation ANG058
Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 ANG059
Angelman Syndrome Due to Maternal 15q11q13 Deletion ANG053
Angelman Syndrome Due to Paternal Uniparental Disomy of Chromosome 15 ANG052
Angel-Shaped Phalangoepiphyseal Dysplasia ANG066
Angelucci's Syndrome ANG003
Angina Pectoris ANG054
Angiocentric Glioma ANG050
Angiodysplasia ANG011
Angiodysplasia of Intestine ANG012
Angioedema ANG015
Angioedema Induced by Ace Inhibitors ANG049
Angioedema, Hereditary, Type I ANG068
Angioedema, Hereditary, Type Iii ANG045
Angioid Streaks ANG004
Angioid Streaks of Choroid ANG008
Angioimmunoblastic Lymphadenopathy with Dysproteinemia ANG025
Angioimmunoblastic T-Cell Lymphoma ANG046
Angiokeratoma ANG016
Angiokeratoma Circumscriptum ANG007
Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas ANG035
Angiokeratoma of Fordyce ANG014
Angiokeratoma of Mibelli ANG006
Angiolipoma ANG017
Angiolipomatosis, Familial ANG063
Angioma Serpiginosum ANG013
Angioma Serpiginosum, Autosomal Dominant ANG028
Angioma Serpiginosum, X-Linked ANG029
Angioma, Hereditary Neurocutaneous ANG067
Angioma, Tufted ANG065
Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert ANG030
Angiomatous Meningioma ANG009
Angiomyolipoma ANG018
Angiomyoma ANG019
Angiomyomatous Hamartoma ANG033
Angioosteohypertrophic Syndrome ANG062
Angioosteohypotrophic Syndrome ANG057
Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps ANG060
Angiosarcoma ANG020
Angiosarcoma of the Scalp ANG034
Angiostrongyliasis ANG002
Angora Hair Nevus ANG056
Angpt1-Related Hereditary Angioedema with Normal C1inh ANG069
Angular Blepharoconjunctivitis ANG010
Angular Cheilitis ANG061
Anhaptoglobinemia ANH003
Anhidrosis ANH002
Anhidrosis, Familial Generalized, with Abnormal or Absent Sweat Glands ANH005
Anhidrosis, Isolated, with Normal Sweat Glands ANH004
Animal Phobia ANM002
Aniridia - Ptosis - Intellectual Disability - Familial Obesity ANR042
Aniridia 1 ANR048
Aniridia 2 ANR047
Aniridia 3 ANR046
Aniridia and Absent Patella ANR043
Aniridia Renal Agenesis Psychomotor Retardation ANR016
Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract ANR049
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation ANR044
Aniridia-Intellectual Disability Syndrome ANR041
Anisakiasis ANS003
Aniseikonia ANS002
Anismus ANS018
Anisocoria ANS021
Anisomastia ANS015
Anisometropia ANS004
Ankrd26-Related Thrombocytopenia ANK019
Ankyloblepharon Filiforme Adnatum and Cleft Palate ANK013
Ankyloblepharon Filiforme Adnatum-Imperforate Anus Syndrome ANK018
Ankyloblepharon Filiforme Imperforate Anus ANK005
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate ANK017
Ankyloglossia ANK008
Ankylosing Vertebral Hyperostosis with Tylosis ANK015
Ankylosis ANK001
Ankylostomiasis ANK010
Annular Atrophic Lichen Planus ANN013
Annular Constricting Bands ANN004
Annular Erythema ANN011
Annular Lichen Planus ANN014
Ano5-Related Muscle Diseases AN5001
Anodontia AND001
Anodontia of Permanent Dentition AND017
Anogenital Venereal Wart ANG005
Anomalous Left Coronary Artery from the Pulmonary Artery ANM031
Anomaly of the Mitral Subvalvular Apparatus ANM025
Anonychia with Flexural Pigmentation ANN015
Anonychia, Total, with Microcephaly ANN018
Anonychia-Ectrodactyly ANN019
Anonychia-Onychodystrophy with Brachydactyly Type B and Ectrodactyly ANN009
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges ANN010
Anophthalmia Cleft Palate Micrognathia ANP013
Anophthalmia Esophageal Atresia Cryptorchidism ANP014
Anophthalmia Megalocornea Cardiopathy Skeletal Anomalies ANP015
Anophthalmos with Limb Anomalies ANP019
Anorchia ANR018
Anorectal Anomalies ANR033
Anorectal Stricture ANR003
Anorexia Nervosa ANR007
Anosmia for Butyl Mercaptan ANS024
Anosmia for Isobutyric Acid ANS022
Anosmia, Isolated Congenital ANS017
Anosognosia ANS006
Anotia Facial Palsy Cardiac Defect ANT029
Anovulation ANV001
Antenatal Bartter Syndrome ANT061
Antenatal Multiminicore Disease with Arthrogryposis Multiplex Congenita ANT052
Anterior Cerebral Artery Infarction ANT004
Anterior Chamber Cleavage Disorder, Cerebellar Hypoplasia, Hypothyroidism, and Tracheal Stenosis ANT065
Anterior Compartment Syndrome ANT010
Anterior Corneal Pigmentation ANT008
Anterior Cranial Fossa Meningioma ANT022
Anterior Cruciate Ligament Tears ANT051
Anterior Cutaneous Nerve Entrapment Syndrome ANT066
Anterior Dislocation of Lens ANT012
Anterior Foramen Magnum Meningioma ANT021
Anterior Horn Cell Disease ANT007
Anterior Optic Tract Meningioma ANT020
Anterior Scleritis ANT023
Anterior Segment Dysgenesis ANT088
Anterior Segment Dysgenesis 1 ANT077
Anterior Segment Dysgenesis 2 ANT086
Anterior Segment Dysgenesis 3 ANT084
Anterior Segment Dysgenesis 4 ANT071
Anterior Segment Dysgenesis 5 ANT085
Anterior Segment Dysgenesis 6 ANT087
Anterior Segment Dysgenesis 7 ANT083
Anterior Segment Dysgenesis 8 ANT067
Anterior Spinal Artery Stroke ANT033
Anterior Spinal Artery Syndrome ANT013
Anterior Urethra Cancer ANT014
Anterior Urethral Valve ANT062
Anterior Uveitis ANT034
Anterograde Amnesia ANT019
Anterolateral Myocardial Infarction ANT001
Anteroseptal Myocardial Infarction ANT005
Anthracosilicosis ANT017
Anthracosis ANT018
Anthracycline Extravasation ANT076
Anthrax Disease ANT024
Anti-Basement Membrane Glomerulonephritis ANT002
Antidepressant or Antipsychotic Toxicity or Dose Selection ANT064
Antidepressant Type Abuse ANT016
Antigen Defined by Monoclonal Antibody Aj9 ANT080
Antigen Defined by Monoclonal Antibody T87 ANT081
Antigen-Peptide-Transporter 2 Deficiency ANT035
Anti-Hla Hyperimmunization ANT036
Anti-P200 Pemphigoid ANT063
Antiphospholipid Syndrome ANT006
Antiphospholipid Syndrome, Familial ANT041
Anti-Pit-1 Antibody Syndrome ANT089
Anti-Plasmin Deficiency, Congenital ANT038
Antipyrine Metabolism ANT078
Antisocial Personality Disorder ANT011
Antisynthetase Syndrome ANT039
Antithrombin Iii Deficiency ANT009
Antithrombin, Familial Hemorrhagic Diathesis Due to ANT082
Antiviral State Repressor, Regulator of ANT079
Antley-Bixler Syndrome ANT003
Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis ANT042
Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis ANT057
Anton's Syndrome ANT040
Anuria ANR004
Anus Adenocarcinoma ANS010
Anus Basaloid Carcinoma ANS001
Anus Benign Neoplasm ANS025
Anus Cancer ANS011
Anus Disease ANS012
Anus Leiomyoma ANS005
Anus Leiomyosarcoma ANS009
Anus Lymphoma ANS007
Anus Rhabdomyosarcoma ANS008
Anus Sarcoma ANS014
Anus, Imperforate ANS023
Anxiety ANX010
Aorta Angiosarcoma ART003
Aorta Atresia ART007
Aorta-Pulmonary Artery Fistula ART027
Aortic Aneurysm ART016
Aortic Aneurysm, Familial Abdominal, 1 ART138
Aortic Aneurysm, Familial Abdominal, 2 ART151
Aortic Aneurysm, Familial Abdominal, 3 ART152
Aortic Aneurysm, Familial Abdominal, 4 ART108
Aortic Aneurysm, Familial Thoracic 1 ART067
Aortic Aneurysm, Familial Thoracic 10 ART134
Aortic Aneurysm, Familial Thoracic 11 ART133
Aortic Aneurysm, Familial Thoracic 2 ART068
Aortic Aneurysm, Familial Thoracic 4 ART028
Aortic Aneurysm, Familial Thoracic 6 ART071
Aortic Aneurysm, Familial Thoracic 7 ART105
Aortic Aneurysm, Familial Thoracic 8 ART107
Aortic Aneurysm, Familial Thoracic 9 ART118
Aortic Arch Anomaly - Peculiar Facies - Intellectual Disability ART113
Aortic Arch Anomaly with Peculiar Facies and Mental Retardation ART029
Aortic Arch Interruption ART030
Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma ART139
Aortic Atherosclerosis ART004
Aortic Coarctation ART031
Aortic Disease ART017
Aortic Dissection Lentiginosis ART032
Aortic Malignant Tumor ART013
Aortic Valve Atresia ART095
Aortic Valve Disease 1 ART115
Aortic Valve Disease 2 ART101
Aortic Valve Dysplasia ART099
Aortic Valve Insufficiency ART018
Aortic Valve Prolapse ART015
Aortic Valves Stenosis of the Child ART033
Aortitis ART012
Aorto-Left Ventricular Tunnel ART097
Aortopulmonary Coronary Arterial Course ART114
Aortopulmonary Window ART034
Aorto-Right Ventricular Tunnel ART098
Aorto-Ventricular Tunnel ART091
Ap-4-Associated Hereditary Spastic Paraplegia AP4001
Apc-Associated Polyposis Conditions APC006
Apert Syndrome APR006
Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal Iv APH014
Aphalangy with Hemivertebrae APH015
Aphasia APH002
Aphonia-Deafness-Retinal Dystrophy-Bifid Halluces-Intellectual Disability Syndrome APH013
Aphthous Stomatitis APH001
Apical Myocardial Infarction APC001
Aplasia Cutis Congenita APL006
Aplasia Cutis Congenita of Limbs Recessive APL009
Aplasia Cutis Congenita of Limbs, Autosomal Recessive APL027
Aplasia Cutis Congenita with Intestinal Lymphangiectasia APL026
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction APL028
Aplasia Cutis Congenita, Nonsyndromic APL023
Aplasia Cutis Myopia APL011
Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy APL029
Aplasia of Lacrimal and Salivary Glands APL002
Aplastic Anemia APL001
Apnea of Prematurity APN006
Apnea, Central Sleep APN007
Apnea, Obstructive Sleep APN008
Apo a-I Deficiency APD001
Apocrine Adenocarcinoma APC004
Apocrine Adenoma APC003
Apocrine Adenosis of Breast APC002
Apocrine Gland Secretion, Variation in APC009
Apocrine Sweat Gland Neoplasm APC005
Apodia APD003
Apoe P.leu167del-Related Lipid Disorders APP012
Apolipoprotein C-Ii Deficiency APL017
Apolipoprotein C-Iii Deficiency APL024
Apparent Mineralocorticoid Excess APP015
Appendiceal L-Cell Glucagon-Like Peptide Producing Tumor APP007
Appendiceal Neoplasm APP003
Appendicitis APP008
Appendicitis, Proneness to APP017
Appendix Adenocarcinoma APP009
Appendix Cancer APP010
Appendix Carcinoid Tumor APP013
Appendix Disease APP018
Appendix Leiomyoma APP005
Appendix Lymphoma APP002
Appendix Mucinous Cystadenocarcinoma APP004
Apperceptive Agnosia APP006
Apple Allergy APP016
Apraxia APR001
Apraxia of Eyelid Opening APR010
Apricot Allergy APR007
Aprosencephaly and Cerebellar Dysgenesis APR008
Aprosencephaly Syndrome APR009
Aquagenic Pruritus AQG001
Aquagenic Syringeal Acrokeratoderma AQG004
Aqueous Misdirection AQS001
Arachindonic Acid, Absence of ARC005
Arachnodactyly - Intellectual Disability - Dysmorphism ARC019
Arachnodactyly-Abnormal Ossification-Intellectual Disability Syndrome ARC020
Arachnoid Cysts ARC007
Arachnoid Cysts, Intracranial ARC025
Arachnoiditis ARC002
Arbitrary Restriction Polymorphism 1 ARB004
Arbovirosis ARB003
Arcus Corneae ARC023
Aredyld ARD001
Aregenerative Anemia ARG006
Arena Syndrome ARN001
Argentine Hemorrhagic Fever ARG001
Argininemia ARG007
Argininosuccinic Aciduria ARG002
Argyll Robertson Pupil ARG003
Argyria ARG004
Arhinia Choanal Atresia Microphthalmia ARH001
Ariboflavinosis ARB001
Arid1b-Related Disorder ARD005
Arima Syndrome ARM010
Arm Folding Preference ARM007
Armfield X-Linked Mental Retardation Syndrome ARM006
Arms, Malformation of ARM008
Arnold Stickler Bourne Syndrome ARN002
Aromatase Deficiency ARM001
Aromatase Excess Syndrome ARM004
Aromatic L-Amino Acid Decarboxylase Deficiency ARM002
Arrhinia ARR002
Arrhythmogenic Right Ventricular Cardiomyopathy ARR042
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 ARR045
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 ARR028
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 ARR027
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 ARR024
Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 ARR041
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 ARR046
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 ARR047
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 ARR048
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 ARR018
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 ARR049
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 ARR050
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 ARR023
Arroyo Garcia Cimadevilla Syndrome ARR003
Arterial Calcification of Infancy ART035
Arterial Calcification, Generalized, of Infancy, 1 ART106
Arterial Calcification, Generalized, of Infancy, 2 ART102
Arterial Dissection with Lentiginosis ART129
Arterial Thoracic Outlet Syndrome ART109
Arterial Tortuosity Syndrome ART001
Arteries, Anomalies of ART140
Arteriolosclerosis ART010
Arteriosclerosis ART021
Arteriosclerosis Obliterans ART008
Arteriosclerosis, Severe Juvenile ART148
Arteriovenous Fistula ART084
Arteriovenous Malformation ART005
Arteriovenous Malformations of the Brain ART141
Arteritic Anterior Ischemic Optic Neuropathy ART110
Arteritis, Familial Granulomatous, with Juvenile Polyarthritis ART142
Arthritis ART022
Arthritis, Sacroiliac ART143
Arthrochalasia Ehlers-Danlos Syndrome ART153
Arthrogryposis and Ectodermal Dysplasia ART037
Arthrogryposis Epileptic Seizures Migrational Brain Disorder ART040
Arthrogryposis Iugr Thoracic Dystrophy ART041
Arthrogryposis Multiplex Congenita Cns Calcification ART043
Arthrogryposis Multiplex Congenita Whistling Face ART048
Arthrogryposis Multiplex Congenita, Neurogenic Type ART127
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect ART137
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death ART051
Arthrogryposis Spinal Muscular Atrophy ART053
Arthrogryposis with Hyperkeratosis ART130
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development ART154
Arthrogryposis, Congenital, Lower Limb, X-Linked ART150
Arthrogryposis, Distal, Type 10 ART112
Arthrogryposis, Distal, Type 1a ART144
Arthrogryposis, Distal, Type 1b ART060
Arthrogryposis, Distal, Type 2a ART061
Arthrogryposis, Distal, Type 2b1 ART155
Arthrogryposis, Distal, Type 2b2 ART156
Arthrogryposis, Distal, Type 2b3 ART157
Arthrogryposis, Distal, Type 2e ART054
Arthrogryposis, Distal, Type 3 ART120
Arthrogryposis, Distal, Type 4 ART131
Arthrogryposis, Distal, Type 5 ART119
Arthrogryposis, Distal, Type 5d ART104
Arthrogryposis, Distal, Type 6 ART128
Arthrogryposis, Distal, Type 7 ART147
Arthrogryposis, Distal, Type 8 ART122
Arthrogryposis, Distal, Type 9 ART146
Arthrogryposis, Distal, with Hypopituitarism, Mental Retardation, and Facial Anomalies ART055
Arthrogryposis, Distal, with Impaired Proprioception and Touch ART136
Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies ART149
Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/palate, and Developmental Delay ART056
Arthrogryposis, Mental Retardation, and Seizures ART103
Arthrogryposis, Perthes Disease, and Upward Gaze Palsy ART135
Arthrogryposis, Renal Dysfunction, and Cholestasis 1 ART062
Arthrogryposis, Renal Dysfunction, and Cholestasis 2 ART063
Arthrogryposis-Like Hand Anomaly and Sensorineural Deafness ART057
Arthropathy ART023
Arthropathy, Erosive ART077
Arthropathy, Progressive Pseudorheumatoid, of Childhood ART116
Arthus Reaction ART006
Artichoke, Modification of Taste by ART145
Articulation Disorder ART014
Arts Syndrome ART002
Arx-Related Intellectual Disability ARX002
Aryepiglottic Fold Cancer ARY001
Aryl Hydrocarbon Hydroxylase Inducibility ARY002
Asah1-Related Disorders ASH005
Asbestos Intoxication ASB003
Asbestosis ASB001
Asbestos-Related Lung Carcinoma ASB002
Ascaridiasis ASC001
Ascaris Lumbricoides Infection ASC010
Ascending Cholangitis ASC003
Ascending Colon Cancer ASC004
Ascites, Chylous ASC009
Aseptic Meningitis ASP003
Aseptic Osteitis ASP023
Asherman's Syndrome ASH001
Askin's Tumor ASK001
Asparagine Synthetase Deficiency ASP024
Asparagus, Specific Smell Hypersensitivity ASP027
Aspartate Aminotransferase, Serum Level of, Quantitative Trait Locus 1 ASP035
Aspartylglucosaminuria ASP002
Asperger Syndrome ASP001
Asperger Syndrome 1 ASP032
Asperger Syndrome 2 ASP031
Asperger Syndrome 3 ASP033
Asperger Syndrome 4 ASP034
Asperger Syndrome, X-Linked 1 ASP028
Asperger Syndrome, X-Linked 2 ASP029
Aspergillosis ASP006
Aspergillus Niger Infection ASP009
Asphyxia Neonatorum ASP004
Asphyxiating Thoracic Dystrophy ASP005
Aspiration Pneumonia ASP007
Aspiration Pneumonitis ASP008
Aspirin Allergy ASP036
Aspirin Resistance ASP030
Asplenia, Isolated Congenital ASP026
Asrar Facharzt Haque Syndrome ASR001
Associative Agnosia ASS001
Astereognosia AST004
Asternia AST008
Asternia with Cardiac, Diaphragmatic, and Abdominal Defects AST009
Asthenopia AST003
Asthma AST005
Asthma, Nasal Polyps, and Aspirin Intolerance AST052
Asthma, Short Stature, and Elevated Iga AST053
Asthma-Related Traits 1 AST055
Asthma-Related Traits 2 AST056
Asthma-Related Traits 3 AST033
Asthma-Related Traits 4 AST034
Asthma-Related Traits 5 AST057
Asthma-Related Traits 6 AST035
Asthma-Related Traits 7 AST032
Asthma-Related Traits 8 AST036
Astigmatism AST006
Astley-Kendall Syndrome AST010
Astrakhan Spotted Fever AST001
Astroblastoma AST002
Astrocytoma AST007
Asymmetric Motor Neuropathy ASY004
Asymmetric Short Stature Syndrome ASY006
Asymptomatic Dengue ASY001
Asymptomatic Neurosyphilis ASY002
Asynchronous Multifocal Osteogenic Sarcoma ASY003
Ataxia - Hypogonadism - Choroidal Dystrophy ATX021
Ataxia and Polyneuropathy, Adult-Onset ATX038
Ataxia Neuropathy Spectrum ATX010
Ataxia with Fasciculations ATX042
Ataxia with Myoclonic Epilepsy and Presenile Dementia ATX043
Ataxia with Vitamin E Deficiency ATX019
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus ATX031
Ataxia, Deafness, and Cardiomyopathy ATX044
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia ATX029
Ataxia, Sensory, 1, Autosomal Dominant ATX023
Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation ATX047
Ataxia-Deafness-Retardation Syndrome ATX037
Ataxia-Microcephaly-Cataract Syndrome ATX045
Ataxia-Oculomotor Apraxia 3 ATX024
Ataxia-Oculomotor Apraxia 4 ATX033
Ataxia-Pancytopenia Syndrome ATX039
Ataxia-Photosensitivity-Short Stature Syndrome ATX036
Ataxia-Telangiectasia ATX030
Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death ATX046
Ataxia-Telangiectasia-Like Disorder 1 ATX040
Ataxia-Telangiectasia-Like Disorder 2 ATX041
Atelosteogenesis ATL001
Atelosteogenesis, Type I ATL011
Atelosteogenesis, Type Ii ATL015
Atelosteogenesis, Type Iii ATL012
Athabaskan Brainstem Dysgenesis Syndrome ATH001
Atheroembolism of Kidney ATH002
Atherosclerosis Susceptibility ATH013
Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease ATH012
Athetosis ATH004
Athrombia, Essential ATH014
Athyreosis ATH010
Atkin-Flaitz Syndrome ATK002
Atlantic Cod Allergy ATL013
Atlantic Salmon Allergy ATL014
Atlanto-Axial Fusion ATL006
Atlantoaxial Subluxation ATL010
Atonic-Astatic Syndrome of Foerster ATN015
Atopic Keratoconjunctivitis ATP013
Atp1a3-Related Neurologic Disorders ATP015
Atp6v0a2-Related Cutis Laxa ATP003
Atp7a-Related Copper Transport Disorders ATP004
Atp8b1 Deficiency ATP014
Atransferrinemia ATR002
Atresia of External Auditory Canal and Conductive Deafness ATR086
Atresia of Small Intestine ATR015
Atresia of Urethra ATR053
Atrial Fibrillation ATR011
Atrial Fibrillation, Familial, 1 ATR026
Atrial Fibrillation, Familial, 10 ATR061
Atrial Fibrillation, Familial, 11 ATR059
Atrial Fibrillation, Familial, 12 ATR069
Atrial Fibrillation, Familial, 13 ATR072
Atrial Fibrillation, Familial, 14 ATR068
Atrial Fibrillation, Familial, 15 ATR092
Atrial Fibrillation, Familial, 18 ATR085
Atrial Fibrillation, Familial, 2 ATR025
Atrial Fibrillation, Familial, 3 ATR038
Atrial Fibrillation, Familial, 4 ATR039
Atrial Fibrillation, Familial, 5 ATR027
Atrial Fibrillation, Familial, 6 ATR035
Atrial Fibrillation, Familial, 7 ATR037
Atrial Fibrillation, Familial, 8 ATR028
Atrial Fibrillation, Familial, 9 ATR070
Atrial Heart Septal Defect ATR010
Atrial Heart Septal Defect 7 ATR093
Atrial Septal Aneurysm ATR055
Atrial Septal Defect 1 ATR062
Atrial Septal Defect 2 ATR066
Atrial Septal Defect 3 ATR022
Atrial Septal Defect 4 ATR031
Atrial Septal Defect 5 ATR023
Atrial Septal Defect 6 ATR034
Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects ATR088
Atrial Septal Defect 8 ATR065
Atrial Septal Defect 9 ATR056
Atrial Septal Defect Coronary Sinus ATR017
Atrial Septal Defect Ostium Primum ATR018
Atrial Septal Defect Sinus Venosus ATR019
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects ATR091
Atrial Standstill ATR081
Atrial Standstill 1 ATR087
Atrial Standstill 2 ATR074
Atrial Tachyarrhythmia with Short Pr Interval ATR048
Atrichia with Papular Lesions ATR013
Atrioventricular Block ATR057
Atrioventricular Dissociation ATR089
Atrioventricular Septal Defect ATR001
Atrioventricular Septal Defect 2 ATR047
Atrioventricular Septal Defect 3 ATR064
Atrioventricular Septal Defect 4 ATR067
Atrioventricular Septal Defect 5 ATR071
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects ATR084
Atrophia Maculosa Varioliformis Cutis, Familial ATR090
Atrophic Flaccid Tympanic Membrane ATR006
Atrophic Gastritis ATR005
Atrophic Glossitis ATR073
Atrophic Lichen Planus ATR052
Atrophic Muscular Disease ATR076
Atrophic Nonflaccid Tympanic Membrane ATR004
Atrophic Rhinitis ATR003
Atrophic Vulva ATR007
Atrophoderma of Pierini and Pasini ATR020
Atrophoderma Vermiculata ATR054
Atrophy of Prostate ATR008
Atrophy of Testis ATR009
Attention Deficit-Hyperactivity Disorder ATT013
Attention Deficit-Hyperactivity Disorder 1 ATT019
Attention Deficit-Hyperactivity Disorder 2 ATT020
Attention Deficit-Hyperactivity Disorder 3 ATT021
Attention Deficit-Hyperactivity Disorder 4 ATT022
Attenuated Chédiak-Higashi Syndrome ATT012
Attenuated Familial Adenomatous Polyposis ATT003
Atypical Autism ATY003
Atypical Breast Papilloma ATY006
Atypical Choroid Plexus Papilloma ATY002
Atypical Chronic Myeloid Leukemia ATY042
Atypical Coarctation of Aorta ATY022
Atypical Depressive Disorder ATY001
Atypical Follicular Adenoma ATY007
Atypical Glycine Encephalopathy ATY025
Atypical Hemolytic-Uremic Syndrome with H Factor Anomaly ATY036
Atypical Juvenile Parkinsonism ATY034
Atypical Lichen Myxedematosus ATY027
Atypical Lipomatous Tumor ATY008
Atypical Meigs Syndrome ATY026
Atypical Mycobacteriosis, Familial ATY012
Atypical Neurofibroma ATY004
Atypical Norrie Disease Due to Monosomy Xp11.3 ATY020
Atypical Polypoid Adenomyoma ATY009
Atypical Teratoid Rhabdoid Tumor ATY005
Atypical Werner Syndrome ATY016
Audiogenic Seizures ADG002
Auditory Agnosia ADT001
Auditory Neuropathy and Optic Atrophy ADT008
Auditory Neuropathy Spectrum Disorder ADT009
Auditory Neuropathy, Autosomal Dominant, 1 ADT007
Auditory System Cancer ADT002
Auditory System Disease ADT003
Au-Kline Syndrome AKL001
Aural Atresia, Congenital ARL004
Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation ARL006
Auricular Abnormalities-Cleft Lip with or Without Cleft Palate-Ocular Abnormalities Syndrome ARC022
Auricular Cancer ARC003
Auriculo-Condylar Syndrome ARC008
Auriculocondylar Syndrome 1 ARC016
Auriculocondylar Syndrome 2 ARC011
Auriculocondylar Syndrome 3 ARC017
Auriculoosteodysplasia ARC009
Aurocephalosyndactyly ARC024
Ausems Wittebol-Post Hennekam Syndrome ASM001
Australia Antigen AST054
Autism ATS364
Autism 10 ATS172
Autism 11 ATS373
Autism 12 ATS374
Autism 13 ATS375
Autism 15 ATS376
Autism 16 ATS377
Autism 17 ATS378
Autism 18 ATS173
Autism 19 ATS170
Autism 3 ATS370
Autism 6 ATS371
Autism 7 ATS372
Autism 8 ATS369
Autism 9 ATS171
Autism Spectrum Disorder ATS007
Autism with Port-Wine Stain ATS014
Autism X-Linked 1 ATS365
Autism X-Linked 2 ATS366
Autism X-Linked 3 ATS367
Autism X-Linked 4 ATS268
Autism X-Linked 5 ATS177
Autism X-Linked 6 ATS358
Autism-Facial Port-Wine Stain Syndrome ATS313
Autoimmune Addison Disease ATM078
Autoimmune Atherosclerosis ATM103
Autoimmune Atrophic Gastritis ATM060
Autoimmune Autonomic Ganglionopathy ATM074
Autoimmune Cardiomyopathy ATM102
Autoimmune Disease ATM095
Autoimmune Disease 1 ATM052
Autoimmune Disease 2 ATM053
Autoimmune Disease 3 ATM054
Autoimmune Disease 4 ATM055
Autoimmune Disease 6 ATM059
Autoimmune Disease of Blood ATM012
Autoimmune Disease of Cardiovascular System ATM013
Autoimmune Disease of Central Nervous System ATM007
Autoimmune Disease of Endocrine System ATM014
Autoimmune Disease of Exocrine System ATM009
Autoimmune Disease of Eyes, Ear, Nose and Throat ATM008
Autoimmune Disease of Gastrointestinal Tract ATM015
Autoimmune Disease of Musculoskeletal System ATM005
Autoimmune Disease of Peripheral Nervous System ATM105
Autoimmune Disease of Skin and Connective Tissue ATM016
Autoimmune Disease of Urogenital Tract ATM018
Autoimmune Disease, Multisystem, Infantile-Onset, 1 ATM094
Autoimmune Disease, Multisystem, Infantile-Onset, 2 ATM093
Autoimmune Disease, Multisystem, with Facial Dysmorphism ATM081
Autoimmune Encephalitis ATM075
Autoimmune Encephalopathy with Parasomnia and Obstructive Sleep Apnea ATM088
Autoimmune Enteropathy ATM020
Autoimmune Gastritis ATM101
Autoimmune Gastrointestinal Dysmotility ATM077
Autoimmune Glomerulonephritis ATM045
Autoimmune Hemolytic Anemia, Warm Type ATM069
Autoimmune Hemolytic Anemia-Autoimmune Thrombocytopenia-Primary Immunodeficiency Syndrome ATM091
Autoimmune Hepatitis ATM011
Autoimmune Hypoparathyroidism ATM068
Autoimmune Inner Ear Disease ATM021
Autoimmune Interstitial Lung, Joint, and Kidney Disease ATM086
Autoimmune Lymphoproliferative Syndrome ATM006
Autoimmune Lymphoproliferative Syndrome Due to Ctla4 Haploinsuffiency ATM087
Autoimmune Lymphoproliferative Syndrome, Type Iia ATM097
Autoimmune Lymphoproliferative Syndrome, Type Iii ATM083
Autoimmune Lymphoproliferative Syndrome, Type V ATM082
Autoimmune Myocarditis ATM022
Autoimmune Neuropathy ATM089
Autoimmune Oophoritis ATM023
Autoimmune Optic Neuritis ATM100
Autoimmune Pancreatitis ATM024
Autoimmune Pancreatitis Type 1 ATM064
Autoimmune Pancreatitis Type 2 ATM063
Autoimmune Peripheral Neuropathy ATM098
Autoimmune Polyendocrine Syndrome ATM019
Autoimmune Polyendocrine Syndrome Type 1 ATM002
Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia ATM096
Autoimmune Polyendocrine Syndrome, Type Ii ATM092
Autoimmune Polyendocrinopathy Type 3 ATM067
Autoimmune Polyendocrinopathy Type 4 ATM066
Autoimmune Polyglandular Syndrome Type 3 ATM061
Autoimmune Progesterone Dermatitis ATM026
Autoimmune Retinopathy ATM076
Autoimmune Thyroid Disease 1 ATM056
Autoimmune Thyroid Disease 2 ATM057
Autoimmune Thyroid Disease 3 ATM050
Autoimmune Thyroid Disease 4 ATM058
Autoimmune Uveitis ATM099
Autoimmune Vasculitis ATM104
Autoimmune-Related Retinopathy and Optic Neuropathy ATM073
Autoinflammation with Arthritis and Dyskeratosis ATN014
Autoinflammation with Infantile Enterocolitis ATN011
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, Plcg2-Associated ATN016
Autoinflammation, Panniculitis, and Dermatosis Syndrome ATN013
Autoinflammatory Syndrome, Familial, Behcet-Like ATN012
Autonomic Nervous System Benign Neoplasm ATN017
Autonomic Nervous System Disease ATN002
Autonomic Nervous System Neoplasm ATN003
Autonomic Neuropathy ATN004
Autonomic Peripheral Neuropathy ATN001
Autosomal Dominant Alport Syndrome ATS015
Autosomal Dominant Café Au Lait Spots ATS270
Autosomal Dominant Cerebellar Ataxia ATS308
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Dgat2 Mutation ATS363
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Kif5a Mutation ATS092
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Tfg Mutation ATS289
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 with Giant Axons ATS241
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2g ATS165
Autosomal Dominant Childhood-Onset Proximal Spinal Muscular Atrophy ATS237
Autosomal Dominant Coarctation of Aorta ATS065
Autosomal Dominant Congenital Stationary Night Blindness ATS168
Autosomal Dominant Deafness-Onychodystrophy Syndrome ATS254
Autosomal Dominant Disease ATS008
Autosomal Dominant Distal Axonal Motor Neuropathy-Myofibrillar Myopathy Syndrome ATS357
Autosomal Dominant Epidermolytic Ichthyosis ATS411
Autosomal Dominant Epilepsy with Auditory Features ATS301
Autosomal Dominant Intellectual Disability 30 ATS348
Autosomal Dominant Intellectual Disability 40 ATS403
Autosomal Dominant Intellectual Disability 49 ATS410
Autosomal Dominant Intermediate Charcot-Marie-Tooth ATS272
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type B ATS261
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease with Neuropathic Pain ATS093
Autosomal Dominant Leukodystrophy with Autonomic Disease ATS309
Autosomal Dominant Limb-Girdle Muscular Dystrophy ATS330
Autosomal Dominant Macrothrombocytopenia ATS208
Autosomal Dominant Mendelian Susceptibility to Mycobacterial Diseases Due to Partial Ifngammar2 Deficiency ATS105
Autosomal Dominant Mental Retardation 55 ATS394
Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome ATS292
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy ATS011
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2 ATS327
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 4 ATS379
Autosomal Dominant Nonsyndromic Deafness ATS005
Autosomal Dominant Nonsyndromic Deafness 34 ATS402
Autosomal Dominant Nonsyndromic Deafness 71 ATS399
Autosomal Dominant Nonsyndromic Deafness 72 ATS400
Autosomal Dominant Nonsyndromic Deafness 73 ATS401
Autosomal Dominant Non-Syndromic Intellectual Disability ATS203
Autosomal Dominant Non-Syndromic Intellectual Disability 1 ATS383
Autosomal Dominant Non-Syndromic Intellectual Disability 19 ATS417
Autosomal Dominant Non-Syndromic Intellectual Disability 2 ATS384
Autosomal Dominant Non-Syndromic Intellectual Disability 3 ATS385
Autosomal Dominant Non-Syndromic Intellectual Disability 4 ATS386
Autosomal Dominant Non-Syndromic Intellectual Disability 5 ATS387
Autosomal Dominant Non-Syndromic Intellectual Disability 6 ATS388
Autosomal Dominant Non-Syndromic Intellectual Disability 8 ATS389
Autosomal Dominant Non-Syndromic Intellectual Disability 9 ATS390
Autosomal Dominant Optic Atrophy and Peripheral Neuropathy ATS077
Autosomal Dominant Optic Atrophy Plus Syndrome ATS069
Autosomal Dominant Palmoplantar Keratoderma and Congenital Alopecia ATS068
Autosomal Dominant Partial Epilepsy with Auditory Features ATS012
Autosomal Dominant Polycystic Kidney Disease ATS347
Autosomal Dominant Preaxial Polydactyly-Upperback Hypertrichosis Syndrome ATS356
Autosomal Dominant Progressive External Ophthalmoplegia ATS025
Autosomal Dominant Proximal Renal Tubular Acidosis ATS111
Autosomal Dominant Robinow Syndrome ATS082
Autosomal Dominant Secondary Polycythemia ATS209
Autosomal Dominant Sideroblastic Anemia 4 ATS407
Autosomal Dominant Spastic Paraplegia Type 9b ATS412
Autosomal Dominant Spinal Muscular Atrophy, Lower Extremity-Predominant 2 ATS418
Autosomal Dominant Tubulointerstitial Kidney Disease ATS382
Autosomal Dominant Tubulointerstitial Kidney Disease Due to Muc1 Mutations ATS419
Autosomal Dominant Tubulointerstitial Kidney Disease Due to Ren Mutations ATS404
Autosomal Dominant Tubulointerstitial Kidney Disease Due to Umod Mutations ATS420
Autosomal Dominant Tubulointerstitial Kidney Disease, Muc1-Related ATS310
Autosomal Dominant Tubulointerstitial Kidney Disease, Ren-Related ATS311
Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related ATS312
Autosomal Genetic Disease ATS009
Autosomal Recessive Alport Syndrome ATS018
Autosomal Recessive Anterior Segment Dysgenesis ATS413
Autosomal Recessive Ataxia Due to Pex10 Deficiency ATS074
Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect ATS421
Autosomal Recessive Cerebellar Ataxia ATS307
Autosomal Recessive Cerebellar Ataxia with Late-Onset Spasticity ATS112
Autosomal Recessive Cerebellar Ataxia-Pyramidal Signs-Nystagmus-Oculomotor Apraxia Syndrome ATS233
Autosomal Recessive Cerebral Atrophy ATS179
Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome ATS314
Autosomal Recessive Complex Spastic Paraplegia Due to Kennedy Pathway Dysfunction ATS405
Autosomal Recessive Congenital Ichthyosis ATS013
Autosomal Recessive Congenital Stationary Night Blindness ATS169
Autosomal Recessive Cutis Laxa Type I ATS393
Autosomal Recessive Cutis Laxa Type Ii Classic Type ATS391
Autosomal Recessive Cutis Laxa Type Iii ATS392
Autosomal Recessive Disease ATS010
Autosomal Recessive Epidermolytic Ichthyosis ATS416
Autosomal Recessive Hypophosphatemic Rickets ATS239
Autosomal Recessive Intellectual Disability 58 ATS360
Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease ATS274
Autosomal Recessive Isolated Optic Atrophy ATS326
Autosomal Recessive Leukoencephalopathy-Ischemic Stroke-Retinitis Pigmentosa Syndrome ATS361
Autosomal Recessive Limb-Girdle Muscular Dystrophy ATS331
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a ATS279
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b ATS298
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c ATS246
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d ATS277
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f ATS297
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g ATS299
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h ATS280
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j ATS207
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l ATS217
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2q ATS211
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2w ATS332
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x ATS333
Autosomal Recessive Malignant Osteopetrosis ATS282
Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita ATS109
Autosomal Recessive Nonsyndromic Congenital Nuclear Cataract ATS022
Autosomal Recessive Nonsyndromic Deafness ATS006
Autosomal Recessive Nonsyndromic Deafness 106 ATS396
Autosomal Recessive Nonsyndromic Deafness 107 ATS397
Autosomal Recessive Nonsyndromic Deafness 108 ATS398
Autosomal Recessive Nonsyndromic Deafness 3 ATS336
Autosomal Recessive Nonsyndromic Deafness 32 ATS409
Autosomal Recessive Nonsyndromic Deafness 36 ATS380
Autosomal Recessive Nonsyndromic Deafness 86 ATS381
Autosomal Recessive Non-Syndromic Intellectual Disability ATS204
Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb ATS252
Autosomal Recessive Palmoplantar Keratoderma and Congenital Alopecia ATS072
Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 ATS406
Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 3 ATS408
Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene ATS075
Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency ATS245
Autosomal Recessive Sideroblastic Anemia ATS210
Autosomal Recessive Spastic Paraplegia Type 59 ATS185
Autosomal Recessive Spastic Paraplegia Type 60 ATS184
Autosomal Recessive Spastic Paraplegia Type 66 ATS190
Autosomal Recessive Spastic Paraplegia Type 67 ATS191
Autosomal Recessive Spastic Paraplegia Type 69 ATS187
Autosomal Recessive Spastic Paraplegia Type 70 ATS188
Autosomal Recessive Spastic Paraplegia Type 71 ATS189
Autosomal Recessive Stickler Syndrome ATS076
Autosomal Recessive Type Iv Ehlers-Danlos Syndrome ATS003
Autosomal Semi-Dominant Severe Lipodystrophic Laminopathy ATS285
Autosomal Thrombocytopenia with Normal Platelets ATS205
Autotopagnosia ATT001
Avascular Necrosis of Femoral Head, Primary, 1 AVS006
Avascular Necrosis of Femoral Head, Primary, 2 AVS005
Avian Influenza AVN001
Avoidant Personality Disorder AVD001
Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities AXN011
Axenfeld-Rieger Syndrome AXN002
Axenfeld-Rieger Syndrome, Type 1 AXN009
Axenfeld-Rieger Syndrome, Type 2 AXN012
Axenfeld-Rieger Syndrome, Type 3 AXN010
Axial Mesodermal Dysplasia Spectrum AXL004
Axial Osteomalacia AXL003
Axillary Adenitis AXL002
Axillary Lipoma AXL001
Axin2-Related Attenuated Familial Adenomatous Polyposis AXN008
Axonal Neuropathy AXN001
Axonal Polyneuropathy Associated with Igg/igm/iga Monoclonal Gammopathy AXN006
Ayazi Syndrome AYZ001
Ayme-Gripp Syndrome AYM001
Azathioprine or 6-Mercatopurine Toxicity or Dose Selection AZT004
Azoospermia AZS001
Azotemia, Familial AZT005
Aztreonam Allergy AZT006
Azygos Continuation of the Inferior Vena Cava AZY001
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