Condition
30,467 condition in the knowledge graph · page 116.
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Catatonia, Malignant
syndrome
disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Catatonia, Organic
phenotype
ICD-10 F06.1
phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Catatonic Rigidity
phenotype
phenotype · Musculoskeletal Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Catatrichy
syndrome
disease · Skin and Connective Tissue Diseases
Catch - Finding of Sensory Dimension of Pain
phenotype
phenotype · Pathological Conditions, Signs and Symptoms
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
syndrome
disease
Catel Manzke Syndrome
syndrome
disease · Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Catheter Infection
syndrome
disease
Catshl Syndrome
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases; Musculoskeletal Diseases
Cauda Equina Paraganglioma
disease
disease
Cauda Equina Syndrome
syndrome
ICD-10 G83.4
disease · Nervous System Diseases
Caudal Appendage
phenotype
phenotype
Caudal Duplication Anomaly
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Caudal Dysgenesis Syndrome
phenotype
phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Caudal Dysplasia Syndrome
syndrome
disease
Caudal Interpedicular Narrowing
phenotype
phenotype
Caudal Regression Syndrome
disease
disease · Musculoskeletal Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Caudate Atrophy
phenotype
phenotype
Causalgia
syndrome
ICD-10 G56.4
disease · Nervous System Diseases
Caused By Mutation In The Tbc1 Domain Family, Member 24 Gene (Tbc1D24, 613577.0004)
phenotype
phenotype
Caused By Mutation In The Transportin 3 Gene (Tnpo3, 610032.0001)
phenotype
phenotype
Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001)
phenotype
phenotype
Cavernous Angioma, Central Nervous System
disease
disease · Cardiovascular Diseases; Neoplasms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases
Cavernous Hemangioma of Brain
disease
disease · Cardiovascular Diseases; Neoplasms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases
Cavernous Hemangioma of Retina
disease
disease · Cardiovascular Diseases; Neoplasms; Hemic and Lymphatic Diseases
Cavernous Hemangioma, Extracerebral
disease
disease · Cardiovascular Diseases; Neoplasms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases
Cavernous Hemangioma, Intracerebral
disease
disease · Cardiovascular Diseases; Neoplasms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases
Cavernous Sinus Meningioma
disease
disease
Cavernous Sinus Syndrome
syndrome
disease · Cardiovascular Diseases; Eye Diseases; Stomatognathic Diseases; Nervous System Diseases
Cavernous Sinus Thrombosis
syndrome
disease · Cardiovascular Diseases; Nervous System Diseases
Cavitary Optic Disc Anomalies
syndrome
disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Cavitation
disease
disease
Cavitation of Lung
syndrome
disease
Cavitation of The Basal Ganglia
syndrome
disease
Cavovarus Deformity of Foot
phenotype
phenotype · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Cchs With Hirschsprung Disease
syndrome
disease · Nervous System Diseases; Respiratory Tract Diseases; Pathological Conditions, Signs and Symptoms
Cd40 Ligand Deficiency
syndrome
disease · Immune System Diseases
Cd59 Deficiency
syndrome
disease · Hemic and Lymphatic Diseases; Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms
Cd8 Deficiency, Familial
syndrome
disease · Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Cdags Syndrome
syndrome
disease · Digestive System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Cecal Neoplasms
group
group · Digestive System Diseases; Neoplasms
Cecum Carcinoma
disease
disease · Digestive System Diseases; Neoplasms
Celiac Disease
syndrome
ICD-10 K90.0
disease · Digestive System Diseases; Nutritional and Metabolic Diseases
Celiac Disease In Children
syndrome
disease
Celiac Disease, Susceptibility To, 4
phenotype
phenotype
Cell Carcinoma
disease
Cellular Angiofibroma
disease
disease · Neoplasms
Cellular Blue Nevus
disease
disease · Neoplasms