Condition

Caries (Morphologic Abnormality)

syndrome

disease · Pathological Conditions, Signs and Symptoms

Carnevale Syndrome

syndrome

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

Carney Complex

syndrome

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

Carney Complex Variant

syndrome

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

Carney Complex, Type 1

syndrome

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

Carney Complex, Type 2

syndrome

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

Carney Triad

syndrome

disease · Digestive System Diseases; Respiratory Tract Diseases; Neoplasms

Carnitine Acetyltransferase Deficiency

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms

Carnitine Deficiency

phenotype

phenotype

Carnitine Palmitoyl Transferase 1A Deficiency

syndrome

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

Carnitine Palmitoyl Transferase 2 Deficiency

syndrome

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

Carnitine Palmitoyltransferase Ii Deficiency, Infantile

syndrome

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

Carnitine Palmitoyltransferase Ii Deficiency, Late-Onset

syndrome

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

Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal

syndrome

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

Carnitine-Acylcarnitine Translocase Deficiency

syndrome

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

Carnosinemia

syndrome

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

Caroli Disease

syndrome

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

Caroli Disease Isolated

syndrome

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

Carotenoids, Plasma Level Of, Quantitative Trait Locus 1

phenotype

phenotype

Carotid Artery Aneurysm

syndrome

ICD-10 I72.0

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Artery Calcification

syndrome

disease

Carotid Artery Dilatation

phenotype

phenotype

Carotid Artery Diseases

group

group · Cardiovascular Diseases; Nervous System Diseases

Carotid Artery Occlusion

phenotype

phenotype · Cardiovascular Diseases; Nervous System Diseases

Carotid Artery Plaque

disease

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Artery Thrombosis

syndrome

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Artery, Internal, Dissection

syndrome

disease · Cardiovascular Diseases; Wounds and Injuries; Nervous System Diseases

Carotid Atherosclerosis

syndrome

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Body Paraganglioma

disease

disease · Neoplasms

Carotid Circulation Transient Ischemic Attack

syndrome

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Disease

syndrome

disease

Carotid Intimal Medial Thickness 1

syndrome

disease · Cardiovascular Diseases

Carotid Paraganglioma

disease

disease

Carotid Pseudoaneurysm

syndrome

disease · Cardiovascular Diseases; Wounds and Injuries; Nervous System Diseases

Carotid Stenosis

syndrome

disease · Cardiovascular Diseases; Nervous System Diseases

Carotid Ulcer

phenotype

phenotype · Cardiovascular Diseases; Nervous System Diseases

Carotid-Cavernous Sinus Fistula

syndrome

disease · Cardiovascular Diseases; Wounds and Injuries; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Carpal Bone Aplasia

phenotype

phenotype

Carpal Bone Hypoplasia

phenotype

phenotype

Carpal Osteolysis

phenotype

phenotype

Carpal Synostosis

disease

disease

Carpal Tunnel Syndrome

syndrome

ICD-10 G56.0

disease · Wounds and Injuries; Nervous System Diseases

Carpal Tunnel Syndrome, Familial

syndrome

disease

Carpenter Syndrome 1

syndrome

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

Carpenter Syndrome 2

syndrome

disease

Carrier Status

phenotype

phenotype

Carrington Syndrome

syndrome

disease · Respiratory Tract Diseases; Hemic and Lymphatic Diseases

Cartilage Destruction

phenotype

phenotype