Achondroplasia Alkaptonuria Aniridia Ataxia Telangiectasia Atrophy, Gyrate Acyltransferase Deficiency, Lecithin:Cholesterol alpha Mannosidosis Adenomatous Polyposis Coli Androgen-Insensitivity Syndrome Adrenoleukodystrophy Angelman Syndrome Achondrogenesis type 2 Acrodermatitis enteropathica Adenine phosphoribosyltransferase deficiency Aspartylglucosaminuria Aciduria, Argininosuccinic Alexander Disease Antithrombin III Deficiencies Arthropathy, progressive pseudorheumatoid, of childhood Allan-Herndon-Dudley syndrome Autoimmune Lymphoproliferative Syndrome ATR-X syndrome Ataxia with vitamin E deficiency Arthrogryposis renal dysfunction cholestasis syndrome Amyotrophic lateral sclerosis 1 Amaurosis congenita of Leber, type 1 Anophthalmos with limb anomalies Acrocallosal Syndrome Amaurosis congenita of Leber, type 2 Acromesomelic dysplasia, Maroteaux type Amaurosis congenita of Leber, type 9 Achromatopsia 2 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Achromatopsia 3 Actin-Accumulation Myopathy Athabaskan brainstem dysgenesis Antenatal Bartter syndrome type 1 Antiplasmin Deficiency Achondrogenesis type 1A Amelogenesis Imperfecta, Type IB Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Amaurosis congenita of Leber, type 5 Alpha-Methylacyl-CoA Racemase Deficiency Axenfeld-Rieger Syndrome, Type 1 Alzheimer Disease Anemia, Aplastic Ataxia, Friedreich's Albinism, Oculocutaneous Alagille Syndrome Alternating hemiplegia of childhood Aicardi-Goutieres syndrome Aceruloplasminemia Alpha-B Crystallinopathy Atrial septal defect 2 Alzheimer disease, familial, type 3 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Axonal Neuropathy, Giant Atrichia with Papular Lesions Alopecia universalis congenita Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Asphyxiating Thoracic Dystrophy 2 Acrocephalosyndactylia Acheiropodia Acrocephalopolysyndactyly Type II Achromatopsia 4 Acromesomelic dysplasia Abetalipoproteinemia alpha-Thalassemia Amyotrophic Lateral Sclerosis Anemia, Sickle Cell Aortic Stenosis, Supravalvular Aarskog Syndrome Adrenocortical Carcinomas Acrofacial dysostosis, Nager type Adrenal hyperplasia, congenital, type 5 Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency Albinism, oculocutaneous, type 2 Acidemias, Propionic Achalasia Addisonianism Alacrimia syndrome Autism Spectrum Disorder Andersen Syndrome Anophthalmia with pulmonary hypoplasia Absent corpus callosum cataract immunodeficiency Ataxia Telangiectasia Like Disorder Arterial Tortuosity Syndrome Alzheimer disease type 2 Aromatase deficiency Amelogenesis Imperfecta, Hypomaturation Type, Iia2 Amelogenesis Imperfecta, Hypomaturation Type, Iia3 Albright hereditary osteodystrophy Activated PI3K-delta Syndrome Apparent mineralocorticoid excess Achondrogenesis type 1B Acromicric dysplasia Allanson Pantzar McLeod syndrome Adenylosuccinate lyase deficiency Aniridia cerebellar ataxia mental deficiency Albinism, Oculocutaneous, Type IV Atelosteogenesis type 2 Amelogenesis imperfecta nephrocalcinosis Absent radii and thrombocytopenia Arts syndrome Al Awadi syndrome Amyotrophic Lateral Sclerosis 4, Juvenile Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Alloimmune Thrombocytopenias, Neonatal Absence Epilepsy Atelosteogenesis, type 1 Aland Island Eye Disease ACTH Deficiency, Isolated Arginine:Glycine Amidinotransferase Deficiency Aplasia of Lacrimal and Salivary Glands Amelogenesis Imperfecta, Type III Autosomal recessive ichthyosis with hypotrichosis Anterior segment mesenchymal dysgenesis Arhinia, choanal atresia, and microphthalmia Acrofacial dysostosis of Weyers Anemia, sideroblastic spinocerebellar ataxia Aphakia, congenital primary Acromelic Frontonasal Dysostosis Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly Arthrogryposis multiplex congenita, distal type 1 Amyotrophic Lateral Sclerosis 8 Autoimmune Lymphoproliferative Syndrome, Type IIA Ablepharon macrostomia syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Amish Infantile Epilepsy Syndrome Arthrogryposis multiplex congenita, distal, X-linked Amish lethal microcephaly Alopecia universalis Alpha-Thalassemia Myelodysplasia Syndrome Auditory Neuropathy, Autosomal Dominant, 1 Acrocapitofemoral Dysplasia Abruzzo Erickson syndrome Amelogenesis Imperfecta, Type IV Ataxia, Spastic, 3, Autosomal Recessive Ataxia, Spastic, 2, Autosomal Recessive Atrial Septal Defect 6 ACRDYS2 Atelosteogenesis Type 3 Adenocarcinoma Adrenal Hyperplasia, Congenital Alcoholism Amelogenesis Imperfecta Anemia Arrhythmia, Cardiac Arthritis, Rheumatoid Asthma Atheroscleroses Atrial Fibrillation Autistic Disorder Atopic Dermatitides Angioedemas, Hereditary Acute Promyelocytic Leukemias Atrophy, Spinal Muscular Aortic Valve, Bicuspid Adenoma, Liver Cell Acrodysostosis Amyloidosis, familial visceral Acatalasia Anemia, Diamond Blackfan Aicardi-Goutieres Syndrome 4 Aicardi-Goutieres Syndrome 3 Aminoacylase 1 deficiency Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Amyotrophic Lateral Sclerosis, Chmp2B-Related Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Atrial Fibrillation, Familial, 3 Ataxia, Sensory, Autosomal Dominant AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency Aortic aneurysm, familial thoracic 4 Acth-Independent Macronodular Adrenal Hyperplasia Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Arterial calcification of infancy Amyotrophic Lateral Sclerosis 2, Juvenile Atrial Fibrillation, Familial, 4 Adult-onset citrullinemia type 2 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Atrial Septal Defect 4 Ataxia, Spastic, 1, Autosomal Dominant Atypical Mycobacteriosis, Familial, X-Linked 2 Atypical Mycobacteriosis, Familial, X-Linked 1 Aortic Aneurysm, Familial Thoracic 6 Amelogenesis Imperfecta, Type Ic Aortic aneurysm, familial thoracic 3 Adenylate Kinase Deficiency, Hemolytic Anemia Due To Amyotrophic Lateral Sclerosis 11 Amyotrophic Lateral Sclerosis 9 Axenfeld-Rieger Syndrome, Type 3 Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency Atrial Septal Defect 5 Aicardi-Goutieres syndrome 5 Amyloidosis, Cerebroarterial, App-Related Aase Smith syndrome 2 ACRDYS1 Atrial Septal Defect 3 Aicardi-Goutieres Syndrome 2 Atrial Septal Defect with Atrioventricular Conduction Defects Autosomal Recessive Primary Microcephaly Aortic Valve Disease 1 Acidosis, Renal Tubular Aromatic amino acid decarboxylase deficiency Anonychia congenita Aural Atresia, Congenital Aortic Valve, Calcification of Azoospermia Auriculo-condylar syndrome Anemia, Hypochromic Microcytic, With Iron Overload Agammaglobulinemia Aneurysms, Aortic Adrenocorticotropic hormone deficiency Adrenocortical Carcinoma, Hereditary Anencephaly ABCD syndrome Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Apolipoprotein C-III Deficiency Anemia, Hemolytic Anemia, Sideroblastic Anxiety Disorder Arthrogryposes Arrest, Heart Aortic Aneurysm, Abdominal Autosomal dominant or sporadic congenital neutropenia Amyloidoses, Familial Atkin syndrome Atrial Standstill Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth Alzheimer disease type 4 Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant Anemia, Diamond-Blackfan, 3 Arthrogryposis multiplex congenita neurogenic type Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Amyotrophic Lateral Sclerosis, Sporadic alpha-Fetoprotein Deficiency Adenosine Triphosphate, Elevated, Of Erythrocytes Amyotrophic Lateral Sclerosis 5 Alpha-ketoglutarate dehydrogenase deficiency Autoimmune polyendocrinopathy syndrome, type 1 Axenfeld-Rieger syndrome Advanced Sleep-Phase Syndrome, Familial Anemia, Dyserythropoietic, Congenital Anorexia Acute Myelomonocytic Leukemias Alveolar capillary dysplasia Apparent Mineralocorticoid Excess Syndrome Atrophies, Muscular Anodontia Afibrinogenemia Adenocarcinoma, Follicular Apneas, Obstructive Sleep Anauxetic dysplasia Angiopathies, Diabetic Amelogenesis imperfecta local hypoplastic form Artery Diseases, Coronary Albuminuria Amnesia Ataxia Axenfeld-Rieger Anomaly Amyloidosis IX Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Anorectal Malformations Adrenal Cortex Neoplasm Adrenal Insufficiencies Alopecia Amyloidoses Anophthalmos Anxiety Aortic Valve Insufficiency Arteriovenous Malformations Asbestoses Autoimmune Diseases Ataxias, Cerebellar Attacks, Transient Ischemic Acute Megakaryoblastic Leukemia Alcoholic Liver Cirrhosis Atrophy, Optic Arteritis, Takayasu Angiopathy, Cerebral Amyloid Ataxia, Spinocerebellar Anemia, hereditary spherocytic hemolytic Acute Lung Injury Acidemia, methylmalonic Arrhythmogenic Right Ventricular Dysplasia Asthenozoospermia Attention Deficit Disorder with Hyperactivity Auditory Neuropathy, Nonsyndromic Recessive Atrial myxoma, familial Arima syndrome Alopecia-Mental Retardation Syndrome 1 Athabaskan severe combined immunodeficiency Acute Kidney Injury Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Alport syndrome, recessive type Adenosine monophosphate deaminase deficiency Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Atrophic Gastritides Anemia, Megaloblastic Astrocytoma Arthritis, Psoriatic Atrioventricular Blocks Anemia, hypochromic microcytic Addisons Disease Arachnodactylies Atrioventricular Canal Defect Adams Oliver syndrome Amyloidosis, Primary Cutaneous Acidosis, Lactic Alopecia Areata Arthritides Agenesis of Corpus Callosum Alcohol Related Disorders Adenocarcinoma Of Esophagus Aneurysm, Dissecting Apnea Aspirin Induced Asthmas Albinism Angiokeratoma Aphasia Arthralgia Atresias, Choanal Athelia Abnormality, Congenital Abnormalities, Multiple Abortion, Spontaneous Acromegaly ACTH Syndrome, Ectopic Adenoma Alveolar Bone Loss Ameloblastoma Anemia, Hemolytic, Congenital Nonspherocytic Anemia, Refractory Angioedemas Anorexia Nervosa Anthracosis Antisocial Personality Disorder Anuria Arnold Chiari Malformation Arterioscleroses Autoimmunities Adenocarcinoma, Bronchiolo-Alveolar Angle Closure Glaucoma Acute Monocytic Leukemias Abuse, Marihuana Acoustic Neuromas Apnea Syndrome, Sleep Albinism, Ocular Affective Disorder, Seasonal Antiphospholipid Syndrome Autoimmune Polyendocrinopathy Anemias, Iron Deficiency Adenomatous Polyps Aging, Premature Alcohol-Induced Disorders Aphasia, Primary Progressive Activated Protein C Resistance Autoimmune Thyroiditides Atrioventricular Septal Defect Ataxia and Polyneuropathy, Adult-Onset Atrial fibrillation, familial 1 Apnea, Postanesthetic Ataxia-Telangiectasia Variant Amelogenesis Imperfecta, Hypomaturation Type, Iia1 Atrial Fibrillation, Familial, 7 Atrial Fibrillation, Familial, 6 Autoimmune Polyendocrinopathy Syndrome, Type I, With Reversible Metaphyseal Dysplasia Amyotrophic Lateral Sclerosis 6, Autosomal Recessive Acquired angioedema Antibody Deficiency due to Defect in CD19 Arthritis, Juvenile Adenomas, Adrenocortical Adrenal Gland Neoplasm ADH Syndrome, Inappropriate Acute Erythroblastic Leukemia Autoimmune Hepatitides Angina, Stable Adiponectin Deficiency Autosomal Dominant Hereditary Pancreatitis Agranulocytoses Anaphylaxis Androblastoma of ovary Aspergers Syndrome Acute fatty liver of pregnancy Acquired Immunodeficiency Syndrome Affective Disorder, Psychotic Anaplasia Abnormalities, Craniofacial Acrodermatitides Alcoholic Intoxication Artery Disease, Carotid Arteritides, Giant Cell Anhedonia Adenocarcinoma, Clear Cell Adenoma, Oxyphilic Aplasia Cutis Congenita with Epibulbar Dermoids Aortic Rupture Apraxias Acute Basophilic Leukemia Angina, Microvascular Asthmas, Occupational Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 1 Auditory neuropathy Antley Bixler Syndrome Phenotype Autosomal Recessive Cerebellar Ataxia Type 1 Abortion, Habitual Abruptio Placentae Acne Vulgaris Adrenal Cortex Disease Alcohol Withdrawal Delirium Anemia, Hypochromic Angina, Unstable Anus, Imperforate Aortic Disease Appendicitis Arthritis, Infectious Aspergilloses Aneurysms, Coronary Acid Deficiencies, Folic Abstinence Syndromes, Neonatal Acquired Hyperostosis Syndrome Aniridia, type 2 Aplastic anemia, idiopathic Amastia Alcohol Withdrawal Seizure Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Acro Osteolysis Angel shaped phalangoepiphyseal dysplasia alpha-2-Macroglobulin Deficiency Abdominal Pain Abnormalities, Drug Induced Abortion, Threatened Acidoses Acute Phase Reaction Adjustment Disorders Adrenal Gland Disease Agricultural Worker Diseases AIDS Dementia Complex Airway Obstruction Alkaloses Allergic Alveolitides, Extrinsic Amenorrhea Amino Acid Metabolism, Inborn Errors Amnesia, Retrograde Anemia, Hemolytic, Autoimmune Anemia, Congenital Hemolytic Anemia, Macrocytic Anemia, Neonatal Anemia, Refractory, with Excess of Blasts Aneuploidies Aneurysms Angina Pectoris Anisometropia Ankyloses Anovulation Anthrax Anus Neoplasm Anxiety, Separation Arenaviridae Infections Arterial Occlusive Disease Arteritides Arthritides, Gouty Ascites Asphyxia Asphyxia Neonatorum Asthenia Auditory Perceptual Disorder Adenocarcinoma, Mucinous Aneurysms, Intracranial Arteriovenous Malformation, Intracranial Aberration, Chromosome Anomalies, Coronary Vessel Abnormalities, Eye Animal Hepatitides Abnormality, Jaw Apparatus Disease, Lacrimal Animal Mammary Neoplasms Abnormality, Mouth Animal Muscular Dystrophies Asthenias, Neurocirculatory Atrophies, Hereditary Optic Abuse, Phencyclidine Aspiration Pneumonias Animal Salmonella Infection Abnormality, Tooth AIDS-Related Lymphomas AIDS-Related Opportunistic Infections Angiolipoma Amphetamine Related Disorders Attention Deficit and Disruptive Behavior Disorders Anaplastic Thyroid Carcinomas Azotemia Atrophodermia reticulata Aase syndrome Acid Phosphatase Deficiency Acetyl-Coa Carboxylase Deficiency Arakawa's syndrome 2 AIDS-related Kaposi sarcoma Arsenic Poisoning Atrophies Artery Dissection, Vertebral Aortic Subvalvular Stenoses Atrial Septal Defect Sinus Venosus Aortic Aneurysm, Familial Thoracic 1 Aganglionosis, total intestinal Atrophy, Multiple System Abnormalities, Lymphatic Amelogenesis Imperfecta hypomaturation type Acrogeria, gottron type Adducted Thumbs Syndrome Angioedema, vibratory Abnormality, Maxillofacial Acute Subdural Hematoma Ataxias, Gait Alcohol-Induced Disorders, Nervous System Autoimmune Diseases of the Nervous System Acromelic frontonasal dysplasia Acromegaloid facial appearance syndrome Anemia, Congenital Hypoplastic Arthritis, Experimental Autonomic Nervous System Diseases Axenfeld Syndrome Amelogenesis imperfecta pigmented hypomaturation type Asymmetries, Facial Agammaglobulinemia, non-Bruton type Alzheimer Disease 9 Ayazi syndrome Albinism ocular late onset sensorineural deafness Agammaglobulinemia, X-linked, type 2 Azoospermia, Nonobstructive Adrenal cyst with ectodermal dysplasia Aortic Aneurysm, Familial Abdominal 1 Amaurosis hypertrichosis Asthma, Nasal Polyps, And Aspirin Intolerance Adrenal Hypoplasia, Cytomegalic Type Acrofacial dysostosis Rodriguez type Absence of tibia with polydactyly Atrial Septal Defect 1 Aneurysm, Intracranial Berry, 1 Alopecia congenita keratosis palmoplantaris Acropectorovertebral Dysplasia, F-Form Abdominal obesity metabolic syndrome Acroosteolysis dominant type Acute erythroleukemia Acute erythroleukemia - M6a subtype Acute myeloid leukemia FAB-M6 Acute erythroleukemia - M6b subtype Alport syndrome, dominant type Achromatopsia incomplete, X-linked Acrocallosal syndrome, Schinzel type Adrenal hyperplasia 2 Aspartylglucosamidase (AGA) deficiency Anti-plasmin deficiency, congenital Acrocephalopolydactylous Dysplasia Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal Amyotrophic Lateral Sclerosis 10 Arteriovenous Fistula Anterior Uveitides Ankyloglossia Acute On Chronic Liver Failure Acanthamoeba Keratitides Aortic Valve Stenoses Ascorbic Acid Deficiencies Aspiration Syndrome, Meconium AIDS Associated Nephropathy Atresias, Tricuspid Atypical Parkinson Disease Acanthosis Nigricans Achlorhydria Actinobacillus Infection Altitude Sickness Amblyopia Aortic Coarctation Arbovirus Infections Arthus Reaction Avian Sarcomas Allergic Conjunctivitides Adenoma, Islet Cell Abscesses, Periapical Aplasia, Pure Red-Cell Animal Toxoplasmoses African Trypanosomiases Alcoholic Neuropathies Annular pancreas Apneas, Central Sleep Atrophy, Geographic Arthrogryposis, Distal, Type 4 Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques Arthrogryposis, distal, type 2E Arthrogryposis, Distal, Type 10 Atrial Septal Defect, Secundum Type Arthrogryposis-like hand anomaly and sensorineural deafness Airway Remodeling Alacrima Atresias, Esophageal Adenocarcinoma, Sebaceous Arrhinia Angiofibroma Autoimmune Lymphoproliferative Syndrome, Type IA Atrophy, Olivopontocerebellar Atrial Complex, Premature Apathy Angioid Streak Anomia Aphasia, Broca Arthropathies, Neurogenic Astigmatism Abscesses, Liver Amaurosis Fugax Artery Stenosis, Pulmonary Amyloidosis, Immunoglobulin Light chain Adrenogenital Syndrome Anetoderma Anodontia of Permanent Dentition Adrenocortical Carcinoma, Pediatric Acantholyses Accidental Fall Acidoses, Respiratory Adenoviridae Infections Aggression Aging Agnosia Agoraphobia AIDS Related Complex Akinetic Mutism Alcohol Drinking Alkaloses, Respiratory Amebiases Anemia, Pernicious Anger Anisocoria Aphonia Arcus Senilis Asthma, Exercise Induced Atelectases, Pulmonary Athetoses Atrial Flutter Ascites, Chylous Acute Disseminated Encephalomyelitides Actinic Keratoses Adenoma, Pleomorphic Aggregation, Platelet Attempted Suicide Arachnoid Cysts Adult Onset Still Disease Addictive Behaviors Amyloid Neuropathies Angiomyolipoma Achromatopsia 1 Amnesia, Transient Global Adenomyosis Absence of septum pellucidum Acute Chest Syndrome Arthritis, Sacroiliac Adiposity Aortic Aneurysm, Familial Thoracic 2 Albinism, Oculocutaneous, Type I, Temperature-Sensitive Anemia, Diamond-Blackfan, 2 Anisomastia Autosomal dominant compelling helio ophthalmic outburst syndrome Autoimmune Lymphoproliferative Syndrome, Type IB Absent patella Aberrant right subclavian artery Attenuated familial adenomatous polyposis Alopecia, Androgenetic, 3 Alopecia, Androgenetic, 2 Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis Achromatopsia 5 Alzheimer disease type 1 Ataxia Neuropathy Spectrum Anti-N-Methyl-D-Aspartate Receptor Encephalitides Anti-Glomerular Basement Membrane Disease Allergic Aspergilloses, Bronchopulmonary Abscess Adenolymphoma Angiodysplasia Anterior Wall Myocardial Infarction Amyopathic dermatomyositis Apraxia, oculomotor, Cogan type Achondrogenesis Attrition, Tooth Acute Pain Amniotic Band Sequence Acute Lung Injury, Transfusion Related Anorchia Angina Pectoris, Variant Aortitides Aphakia Arthritides, Reactive Acute Cholecystitis Alveolar echinococcosis Adenoma, Villous Adenomatoid Tumor Actinic cheilitis Autoimmune enteropathy Actinic Prurigo Autoimmune limbic encephalitis Adenocarcinoma, Papillary Affective Symptom Amebic Dysenteries Aneurysm, Ruptured Avitaminoses Acute Generalized Exanthematous Pustulosis Askin Tumor Adamantinoma Aryl Hydrocarbon Hydroxylase Inducibility Acrospiromas Amyloidosis, Cerebral, with Spongiform Encephalopathy Amyloid angiopathy Amyotrophic lateral sclerosis, type 6 Acquired CJD Abdominal Neoplasm Adenosarcoma Amputation Stumps Angiolymphoid Hyperplasia with Eosinophilia Appendiceal Neoplasm Apudoma Arteriosclerosis Obliterans Adenocarcinoma, Scirrhous Abscess, Amebic Liver Aphthous Stomatitides Alphavirus Infections Autonomic Dysreflexia Aagenaes syndrome Adenocarcinoid tumor Adenoameloblastoma Autoimmune Hypophysitis Anal Canal Carcinoma Arterioloscleroses Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities Alzheimer Disease 10 Alzheimer Disease 5 Alzheimer Disease 12 Acquired Protein S Deficiency Antisynthetase syndrome Adrenal incidentaloma Acute malaria Acquired amegakaryocytic thrombocytopenia Adrenal Insufficiency, Congenital Abdomen, Acute Acinetobacter Infection Acne Keloid Actinomycoses Adenofibroma Adenoma, Chromophobe Adenoma, Acidophil Adiposis Dolorosa Adnexal Disease Adrenal Rest Tumor African Swine Fever Agraphia Aleutian Mink Disease Anaplasmoses Ancylostomiases Anemia, Myelophthisic Angiomatoses Aniseikonia Anthracosilicoses Aortopulmonary Septal Defect Arachnoiditides Articulation Disorder Ascariases Arterioscleroses, Intracranial Abuse, Child Sexual Adenoma, Bile Duct Acute Hemorrhagic Conjunctivitides Amniotic Fluid Embolisms American Hemorrhagic Fever Adenoma, Sweat Gland Acute Eosinophilic Leukemia Abscesses, Lung Abscesses, Periodontal Abscesses, Peritonsillar Accreta, Placenta Aberration, Sex Chromosome Asthmaticus, Status Atrial Ectopic Tachycardias Accelerated Idioventricular Rhythm Abscesses, Psoas Angiomatoses, Bacillary Ankyloses, Tooth Anisakiasis Abdominal Hernia Arterivirus Infections Adenomyoma Angiomyoma Anterior Spinal Artery Syndrome Atrophic Vaginitis Apraxia, Ideomotor Annular Erythema Abdominal Abscess Acne Conglobatas Angiostrongylus cantonensis infection Angiostrongyliasis Anxiety, Performance Acrokeratoelastoidosis of Costa Acute zonal occult outer retinopathy Appearance, Body Physical Acanthoma Alice in Wonderland Syndrome Adenomyoepithelioma Ankyloblepharon filiforme adnatum Angiosarcoma of the breast Acanthocheilonemiases Atrophia Maculosa Varioliformis Cutis, Familial Al-Gazali Syndrome Ambras syndrome Acute Tubulointerstitial Nephritis Alopecia Areata 2 Alzheimer Disease 7 Arthropathy, Erosive Alzheimer Disease 6 Asthma and Nasal Polyps Acrofrontofacionasal dysostosis syndrome Adult i Blood Group Phenotype Ankyloblepharon Filiforme Adnatum and Cleft Palate Amyotrophic Lateral Sclerosis, Autosomal Recessive Alzheimer Disease, Familial, 1 Alzheimer Disease 14 Adenosarcoma of the uterus Ageusia Achondroplastic dwarfism alpha-1-Antitrypsin Deficiency, Autosomal Recessive African Hemochromatosis Acute Febrile Encephalopathies Adrenal Cortex Aorta Artery Autophagy Axon Arterial Disease, Cerebral Atrium, Heart Auricle, Ear Atrial Fibrillation, Familial, 5 Albinism, minimal pigment type