Condition

Autoinflammatory Disease

syndrome

disease

Autoinflammatory Disorder

syndrome

disease

Autoinflammatory Syndrome

syndrome

disease · Pathological Conditions, Signs and Symptoms

Autoinflammatory Syndrome, Familial, Behcet-Like

syndrome

disease

Autologous Graft Versus Host Disease

syndrome

disease

Autonomic Bladder Dysfunction

syndrome

disease · Nervous System Diseases

Autonomic Dysreflexia

syndrome

disease · Nervous System Diseases

Autonomic Erectile Dysfunction

phenotype

phenotype · Nervous System Diseases

Autonomic Hyperreflexia of Bladder

syndrome

disease · Nervous System Diseases

Autonomic Nervous System Disorders

group

ICD-10 G90; G90.9

group · Nervous System Diseases

Autonomic Nervous System Dysfunction

phenotype

phenotype

Autonomic Nervous System Imbalance

syndrome

disease · Nervous System Diseases

Autonomic Neuropathy

syndrome

disease · Nervous System Diseases

Autonomous Thyroid Function

syndrome

disease · Endocrine System Diseases

Autophagic Vaculoes (Finding)

phenotype

phenotype

Autoresuscitation

phenotype

phenotype

Autosomal Agammaglobulinemia With Absent B-Cells

syndrome

disease · Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Autosomal Aneuploidy

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Chromosome Disorders

group

group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Beta2-Microglobulinic Amyloidosis

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Autosomal Dominant Cerebellar Ataxia

syndrome

disease

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Kif5A Mutation

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2D

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Autosomal Dominant Compelling Helio Ophthalmic Outburst Syndrome

syndrome

disease · Pathological Conditions, Signs and Symptoms

Autosomal Dominant Contiguous Gene Syndrome

syndrome

disease

Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder)

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases

Autosomal Dominant Epidermolysis Bullosa Simplex

syndrome

disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Familial Dystonia

syndrome

disease · Nervous System Diseases

Autosomal Dominant Focal Segmental Glomerulosclerosis

syndrome

disease · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications

Autosomal Dominant Hereditary Pancreatitis

syndrome

disease · Digestive System Diseases

Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency

syndrome

disease · Nutritional and Metabolic Diseases

Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency

syndrome

disease · Nutritional and Metabolic Diseases

Autosomal Dominant Hypocalcemia

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Syndrome (Disorder)

syndrome

disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Hypophosphatemic Rickets

syndrome

disease · Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Male Urogenital Diseases; Musculoskeletal Diseases

Autosomal Dominant Ichthyosis

disease

disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Ichthyosis Vulgaris

disease

disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Autosomal Dominant Juvenile Parkinson Disease

syndrome

disease · Nervous System Diseases

Autosomal Dominant Keratitis

syndrome

disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Late Onset Parkinson Disease

syndrome

disease · Nervous System Diseases

Autosomal Dominant Lateral Temporal Lobe Epilepsy

syndrome

disease · Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A

syndrome

disease

Autosomal Dominant Macrothrombocytopenia

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Autosomal Dominant Myotubular Myopathy

syndrome

disease · Nervous System Diseases; Musculoskeletal Diseases

Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Autosomal Dominant Neurohypophyseal Diabetes Insipidus

syndrome

disease · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases

Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

syndrome

disease · Nervous System Diseases