Condition

Al Awadi Syndrome

syndrome

disease · Musculoskeletal Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms

Al Kaissi Syndrome

syndrome

disease

Al-Gazali Syndrome

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Al-Raqad Syndrome

syndrome

disease

Alacrima

syndrome

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

Alacrima, Achalasia, And Mental Retardation Syndrome

syndrome

disease

Alacrima, Congenital, Autosomal Recessive

syndrome

disease

Alagille Syndrome

disease

disease · Cardiovascular Diseases; Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Alagille Syndrome 1

syndrome

disease · Cardiovascular Diseases; Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Alagille Syndrome 2

syndrome

disease · Cardiovascular Diseases; Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Alanine Aminotransferase Increased

phenotype

phenotype · Digestive System Diseases

Alanine Aminotransferase Measurement

phenotype

phenotype

Alanine Measurement

phenotype

phenotype

Alazami-Yuan Syndrome

syndrome

disease

Albers-Schonberg Disease, Autosomal Recessive

syndrome

disease · Musculoskeletal Diseases

Albinism

syndrome

ICD-10 E70.3

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

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases

Albinism, Ocular

disease

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

Albinism, Ocular, With Late-Onset Sensorineural Deafness (Disorder)

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases

Albinism, Ocular, With Sensorineural Deafness (Disorder)

syndrome

disease

Albinism, Oculocutaneous

disease

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

Albinism, Oculocutaneous, Type I, Temperature-Sensitive

syndrome

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

Albinism, Oculocutaneous, Type Ib (Disorder)

syndrome

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

Albinism, Oculocutaneous, Type Iii

syndrome

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

Albinism, Oculocutaneous, Type V

syndrome

disease

Albinism, Oculocutaneous, Type Vi

syndrome

disease

Albinism, Oculocutaneous, Type Vii

syndrome

disease

Albinism, Tyrosinase-Negative

disease

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

Albinism, Tyrosinase-Positive

disease

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

Albinism, Yellow-Mutant

phenotype

phenotype · Eye Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Albinoidism, Oculocutaneous, Autosomal Dominant

syndrome

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

Albright'S Hereditary Osteodystrophy

syndrome

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

Albumin B Phenotype

phenotype

phenotype

Albumin Blenheim Phenotype

phenotype

phenotype

Albuminuria

phenotype

phenotype · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms

Alcohol Abuse

disease

disease · Mental Disorders; Chemically-Induced Disorders

Alcohol Abuse Or Dependence

disease

disease

Alcohol Consumption

phenotype

ICD-10 Z72.1

phenotype · Behavior and Behavior Mechanisms

Alcohol Consumption During Pregnancy

phenotype

phenotype

Alcohol Dependence With Withdrawal, Unspecified

disease

disease · Mental Disorders; Chemically-Induced Disorders

Alcohol Dependence, Protection Against

phenotype

phenotype

Alcohol Dependence, Susceptibility To

phenotype

phenotype

Alcohol Effect

phenotype

phenotype

Alcohol Flush Reaction

phenotype

phenotype · Mental Disorders; Chemically-Induced Disorders; Pathological Conditions, Signs and Symptoms

Alcohol Myopathy

syndrome

ICD-10 G72.1

disease · Mental Disorders; Chemically-Induced Disorders; Nervous System Diseases; Musculoskeletal Diseases

Alcohol Or Other Drugs Use

disease

disease

Alcohol Problem

phenotype

phenotype

Alcohol Related Birth Defect

syndrome

disease · Chemically-Induced Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications