Condition
30,467 condition in the knowledge graph · page 124.
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Chalasia of Lower Esophageal Sphincter
syndrome
disease · Digestive System Diseases
Chancroids
syndrome
ICD-10 A57
disease · Male Urogenital Diseases; Infections; Female Urogenital Diseases and Pregnancy Complications
Chandler Syndrome
syndrome
disease · Eye Diseases
Change In Stool Consistency
phenotype
phenotype
Change In Voice (Finding)
phenotype
phenotype · Nervous System Diseases; Otorhinolaryngologic Diseases; Respiratory Tract Diseases; Pathological Conditions, Signs and Symptoms
Channelopathies
syndrome
disease · Pathological Conditions, Signs and Symptoms
Chapping of Lips
phenotype
phenotype · Stomatognathic Diseases
Char Syndrome
syndrome
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Charcot Gait
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Charcot-Marie-Tooth Disease
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease And Deafness
syndrome
disease · Otorhinolaryngologic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Charcot-Marie-Tooth Disease Type 2B5
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease Type 4
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease Type 4B3
syndrome
disease
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2K
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2A2A
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2K, Modifier of (1 Family)
phenotype
phenotype
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2A2B
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2A1
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 (Disorder)
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2A2A
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2B (Disorder)
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2Cc
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2Dd
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2E (Disorder)
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2F
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2G
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2K
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2L (Disorder)
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2N
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Axonal, Type 2O
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2P
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2Q
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2R
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2S
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2T
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2U
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2V
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2W
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2X
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2Y
syndrome
disease
Charcot-Marie-Tooth Disease, Axonal, Type 2Z
syndrome
disease
Charcot-Marie-Tooth Disease, Demyelinating, Type 1E
syndrome
disease · Otorhinolaryngologic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Charcot-Marie-Tooth Disease, Demyelinating, Type 1F
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Demyelinating, Type 1G
syndrome
disease
Charcot-Marie-Tooth Disease, Demyelinating, Type 4F
syndrome
disease
Charcot-Marie-Tooth Disease, Dominant Intermediate A
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Charcot-Marie-Tooth Disease, Dominant Intermediate B (Disorder)
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases