Condition

Abdominal Bloating

phenotype

phenotype · Digestive System Diseases

Abdominal Cocoon

syndrome

disease

Abdominal Colic

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Abdominal Compartment Syndrome

syndrome

disease · Cardiovascular Diseases; Musculoskeletal Diseases

Abdominal Cramps

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Abdominal Cryptorchidism

disease

disease · Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases

Abdominal Discomfort

phenotype

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

Abdominal Infection

group

group · Infections

Abdominal Mass

phenotype

phenotype · Digestive System Diseases

Abdominal Migraine

syndrome

disease · Nervous System Diseases

Abdominal Neoplasms

group

group · Neoplasms

Abdominal Obesity Metabolic Syndrome

syndrome

disease · Nutritional and Metabolic Diseases

Abdominal Obesity-Metabolic Syndrome 1

syndrome

disease · Nutritional and Metabolic Diseases

Abdominal Obesity-Metabolic Syndrome 3

syndrome

disease

Abdominal Pain

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Abdominal Pain In Children

phenotype

phenotype

Abdominal Sepsis

syndrome

disease

Abdominal Situs Ambiguus

phenotype

phenotype

Abdominal Stoma

disease

disease

Abdominal Symptom

phenotype

phenotype

Abdominal Tenderness

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Abdominal Tuberculosis

syndrome

disease

Abdominal Wall Defect

group

group

Abdominal Wall Infection

syndrome

disease

Abdominal Wall Muscle Weakness

phenotype

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

Abducens Nerve Palsy

syndrome

ICD-10 H49.2

disease · Nervous System Diseases

Aberrant Crypt Foci

phenotype

phenotype · Neoplasms

Aberrant Melanosome Maturation

phenotype

phenotype

Aberrant Right Subclavian Artery

disease

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

Abetalipoproteinemia

syndrome

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

Abiotrophy

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Ablepharon

disease

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

Ablepharon-Macrostomia Syndrome

syndrome

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

Abnormal Activity of Mitochondrial Respiratory Chain

phenotype

phenotype

Abnormal Adipose Tissue Morphology

disease

disease

Abnormal Aggressive, Impulsive Or Violent Behavior

phenotype

phenotype · Behavior and Behavior Mechanisms

Abnormal Albumin Level

phenotype

phenotype

Abnormal Aldolase Level

phenotype

phenotype

Abnormal Alpha Granule Content

phenotype

phenotype

Abnormal Amniotic Fluid

phenotype

phenotype

Abnormal Amplitude of Pattern Reversal Visual Evoked Potentials

phenotype

phenotype

Abnormal Aortic Morphology

disease

disease

Abnormal Aortic Valve Physiology

syndrome

disease

Abnormal Apolipoprotein Level

phenotype

phenotype

Abnormal Atrioventricular Conduction

phenotype

phenotype

Abnormal Auditory Evoked Potential

phenotype

phenotype

Abnormal Axonemal Organization of Respiratory Motile Cilia

disease

disease

Abnormal B Cell Count

phenotype

phenotype