Condition

Aqueous Humor Disorders

syndrome

disease · Eye Diseases

Arachidonic Acid Measurement

phenotype

phenotype

Arachnodactyly

disease

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

Arachnoid Cysts

syndrome

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

Arachnoid Hemangiomatosis

phenotype

phenotype · Neoplasms

Arachnoid Web

syndrome

disease

Arachnoiditis

syndrome

disease · Nervous System Diseases

Arachnophobia

disease

disease · Mental Disorders

Arakawa Syndrome 2

syndrome

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

Arbovirus Infections

group

group · Infections

Arcus Senilis

syndrome

disease · Eye Diseases

Arcus Senilis, Bilateral

syndrome

disease · Eye Diseases

Areas of Hypopigmentation And Hyperpigmentation That Do Not Follow Blaschko Lines

phenotype

phenotype

Areflexia of Lower Limbs

phenotype

phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Areflexia of Upper Limbs

phenotype

phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Arenaviridae Infections

group

group · Infections

Argentaffinoma

disease

disease · Neoplasms

Arginine:Glycine Amidinotransferase Deficiency

syndrome

disease · Mental Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Behavior and Behavior Mechanisms; Pathological Conditions, Signs and Symptoms

Argininosuccinic Acid Synthetase Deficiency Disease, Partial

syndrome

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

Argininosuccinic Acid Synthetase Deficiency, Complete

syndrome

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

Argininosuccinic Aciduria

syndrome

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

Argininuria

phenotype

phenotype

Argyrophilic Grain Disease

syndrome

disease

Arhinencephaly

disease

ICD-10 Q04.1

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

Arhinia, Choanal Atresia, And Microphthalmia

syndrome

disease · Eye Diseases; Otorhinolaryngologic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases

Aria-H

syndrome

disease

Arima Syndrome

syndrome

disease · Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Male Urogenital Diseases

Aristolochic Acid Nephropathy

syndrome

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

Arm Pain

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Arm Span

phenotype

phenotype

Arnold Chiari Malformation

disease

ICD-10 Q07.0

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

Arnold-Chiari Malformation, Type I

disease

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

Arnold-Chiari Malformation, Type Iii

disease

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

Arnold-Chiari Malformation, Type Iv

disease

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

Arnold-Chiari Syndrome, Type Iv

syndrome

disease

Aromatase Deficiency

syndrome

disease · Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System Diseases

Aromatase Excess Syndrome

syndrome

disease · Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System Diseases

Aromatic Amino Acid Decarboxylase Deficiency

syndrome

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

Arrest of Spermatogenesis

phenotype

phenotype · Male Urogenital Diseases

Arrested Hydrocephalus

syndrome

disease · Nervous System Diseases

Arrhinia

disease

ICD-10 Q30.1

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Arrhythmogenic Right Ventricular Dysplasia

syndrome

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

Arrhythmogenic Right Ventricular Dysplasia 1

phenotype

phenotype

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 (Disorder)

syndrome

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10

syndrome

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11

syndrome

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, With Mild Palmoplantar Keratoderma And Woolly Hair

syndrome

disease

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, With Or Without Mild Palmoplantar Keratoderma

syndrome

disease