Condition

Central Nervous System Sensitization

syndrome

disease

Central Nervous System Vascular Malformations

group

group · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Central Nervous System Viral Diseases

group

ICD-10 A80-A89.9; A89

group · Infections; Nervous System Diseases

Central Neuroblastoma

disease

disease · Nervous System Diseases; Neoplasms

Central Neurocytoma

disease

disease · Nervous System Diseases; Neoplasms

Central Neuropathic Pain

syndrome

disease

Central Odontogenic Fibroma

disease

disease · Neoplasms

Central Opacification of The Cornea

phenotype

phenotype

Central Pain

phenotype

phenotype · Mental Disorders; Pathological Conditions, Signs and Symptoms

Central Pain Syndrome

syndrome

disease · Nervous System Diseases

Central Post-Stroke Pain

phenotype

phenotype

Central Precocious Puberty

syndrome

disease · Endocrine System Diseases

Central Retinal Artery Occlusion

syndrome

ICD-10 H34.1

disease · Cardiovascular Diseases; Eye Diseases

Central Retinal Vein Occlusion

syndrome

disease · Cardiovascular Diseases; Eye Diseases; Nervous System Diseases

Central Retinal Vein Occlusion - Juvenile

disease

disease

Central Retinal Vessel Vascular Tortuosity

phenotype

phenotype

Central Serous Chorioretinopathy

syndrome

disease · Eye Diseases

Central Sleep Apnea Syndrome

syndrome

disease · Nervous System Diseases; Mental Disorders; Respiratory Tract Diseases; Pathological Conditions, Signs and Symptoms

Central Topographic Island

syndrome

disease

Central Vertebral Hypoplasia

phenotype

phenotype

Central Visual Impairment

syndrome

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

Central Y-Shaped Metacarpal

phenotype

phenotype

Centrally Nucleated Skeletal Muscle Fibers

phenotype

phenotype

Centriacinar Emphysema

syndrome

ICD-10 J43.2

disease · Respiratory Tract Diseases

Centripetalis Recessive Dystrophic Epidermolysis Bullosa

syndrome

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

Centrocytic (Mantle Cell) Lymphoma (Kiel Classification)

disease

disease

Centrocytic Lymphoma

disease

disease

Centronuclear Myopathy

syndrome

disease · Nervous System Diseases; Musculoskeletal Diseases

Cephalhematoma Due To Birth Trauma

phenotype

ICD-10 P12.0

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

Cephalohematoma

phenotype

phenotype

Cerebellar Agenesis

disease

disease

Cerebellar Ataxia

phenotype

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

Cerebellar Ataxia And Hypogonadotropic Hypogonadism

syndrome

disease · Endocrine System Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cerebellar Ataxia And Mental Retardation With Quadrupedal Locomotion 1

disease

disease

Cerebellar Ataxia Associated With Quadrupedal Gait

phenotype

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

Cerebellar Ataxia With Neuropathy And Bilateral Vestibular Areflexia Syndrome

syndrome

disease

Cerebellar Ataxia, Cataract, And Diabetes Mellitus

disease

disease

Cerebellar Ataxia, Cayman Type

syndrome

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

Cerebellar Ataxia, Deafness, And Narcolepsy

syndrome

disease · Mental Disorders; Otorhinolaryngologic Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant

syndrome

disease

Cerebellar Ataxia, Early Onset

syndrome

ICD-10 G11.1

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

Cerebellar Ataxia, Intellectual Disability, Oculomotor Apraxia, Cerebellar Cysts Syndrome

syndrome

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

Cerebellar Ataxia, Late Onset

syndrome

ICD-10 G11.2

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

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 1

syndrome

disease · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2

syndrome

disease · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3

syndrome

disease · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 4

syndrome

disease

Cerebellar Ataxia, Neuropathy, And Vestibular Areflexia Syndrome

syndrome

disease