Condition

Benzodiazepine Abuse

phenotype

phenotype

Beriberi

syndrome

ICD-10 E51.1

disease · Nutritional and Metabolic Diseases

Bernard-Soulier Syndrome

syndrome

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

Bernard-Soulier Syndrome, Type A1

syndrome

disease

Bernard-Soulier Syndrome, Type A2, Autosomal Dominant

syndrome

disease

Bernard-Soulier Syndrome, Type B

syndrome

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

Bernard-Soulier Syndrome, Type C

syndrome

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

Berry Aneurysm

disease

disease · Cardiovascular Diseases; Nervous System Diseases

Berylliosis

disease

ICD-10 J63.2

disease · Occupational Diseases; Respiratory Tract Diseases

Beryllium Disease

syndrome

disease · Occupational Diseases; Respiratory Tract Diseases

Beryllium Disease, Chronic, Susceptibility To

phenotype

phenotype

Besnoitiasis

syndrome

disease · Infections

Best Vitelliform Macular Dystrophy, Multifocal (Disorder)

syndrome

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

Bestrophinopathy

syndrome

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

Bestrophinopathy, Autosomal Recessive

syndrome

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

Beta Globulin Measurement

phenotype

phenotype

Beta Haemolytic Streptococcal Infection

syndrome

disease · Infections

Beta Thalassemia

syndrome

ICD-10 D56.1

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

Beta Thalassemia Intermedia

syndrome

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

Beta Thalassemia Minor

syndrome

disease

Beta Thalassemia Trait

syndrome

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

Beta Thalassemia, Dominant Inclusion Body Type

syndrome

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

Beta Thalassemia, Heterozygous

syndrome

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

Beta^+^ Thalassemia

syndrome

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

Beta^0^ Thalassemia

syndrome

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

Beta-2-Microglobulin Measurement

phenotype

phenotype

Beta-Aminoisobutyric Acid, Urinary Excretion Of

syndrome

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

Beta-Catenin-Activated Hepatocellular Adenoma

disease

disease · Digestive System Diseases; Neoplasms

Beta-Cell Dysfunction

phenotype

phenotype

Beta-Eeg

phenotype

phenotype

Beta-Endorphin Measurement

phenotype

phenotype

Beta-Galactosidase Deficiency

syndrome

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

Beta-Glucopyranoside Tasting

phenotype

phenotype

Beta-Hexosaminidase A, Pseudodeficiency Of

syndrome

disease

Beta-Hydroxyisobutyryl Coa Deacylase Deficiency

syndrome

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

Beta-Knossos-Thalassemia

disease

disease

Beta-Malay-Thalassemia

disease

disease

Beta-Mannosidosis

syndrome

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

Beta-Plus-Thalassemia, Dominant

disease

disease

Beta-Sarcoglycanopathy

syndrome

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

Beta-Showa-Yakushiji Thalassemia

disease

disease

Beta-Thalassemia Intermedia, Dominant

syndrome

disease

Beta-Thalassemia, Lermontov Type

disease

disease

Beta-Ureidopropionase Deficiency

syndrome

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

Bethlem Myopathy 1

syndrome

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

Bethlem Myopathy 1, Autosomal Recessive

syndrome

disease

Bethlem Myopathy 2

syndrome

disease

Biallelic Rpe65 Mutation Associated Retinal Dystrophy

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities