serw-MX  [xml]  

 DeCS Categories

C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.762 Perceptual Disorders .
C10.597.606.762.300 Hallucinations .
C10.597.606.762.300.500 Charles Bonnet Syndrome .
C11 Eye Diseases .
C11.204 Corneal Diseases .
C11.204.497 Iridocorneal Endothelial Syndrome .
C11.941 Uveal Diseases .
C11.941.375 Iris Diseases .
C11.941.375.322 Iridocorneal Endothelial Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.239 CHARGE Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.165 CHARGE Syndrome .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.800 Adrenocortical Hyperfunction .
C19.053.800.604 Hyperaldosteronism .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.604 Neurobehavioral Manifestations .
C23.888.592.604.764 Perceptual Disorders .
C23.888.592.604.764.300 Hallucinations .
C23.888.592.604.764.300.500 Charles Bonnet Syndrome .
F01 Behavior and Behavior Mechanisms .
F01.700 Neurobehavioral Manifestations .
F01.700.750 Perceptual Disorders .
F01.700.750.300 Hallucinations .
F01.700.750.300.500 Charles Bonnet Syndrome .
 Synonyms & Historicals
Charles Bonnet Syndrome .
Repetitive visual hallucinations experienced mostly by elderly with diminished visual acuity or visual field loss, with awareness of the fictional nature of their hallucinations. It is not associated with delusions and other sensory hallucinations. .
CHARGE Syndrome .
CHARGE Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies .
Hall-Hittner Syndrome .
Association, CHARGE .
Associations, CHARGE .
CHARGE Associations .
CHARGE Syndrome, Familial .
CHARGE Syndromes .
CHARGE Syndromes, Familial .
Familial CHARGE Syndromes .
Hall Hittner Syndrome .
Syndrome, CHARGE .
Syndrome, Hall-Hittner .
CHARGE Association .
Familial CHARGE Syndrome .
Rare disease characterized by COLOBOMA; CHOANAL ATRESIA; and abnormal SEMICIRCULAR CANALS. Mutations in CHD7 protein resulting in disturbed neural crest development are associated with CHARGE Syndrome. .
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
A characteristic symptom complex. .
Iridocorneal Endothelial Syndrome .
Chandler Syndrome .
Chandler's Syndrome .
Dystrophy Endothelial Cornea .
Iris Atrophy with Corneal Edema and Glaucoma .
Chandlers Syndrome .
Cornea, Dystrophy Endothelial .
Corneas, Dystrophy Endothelial .
Dystrophy Endothelial Corneas .
Endothelial Cornea, Dystrophy .
Endothelial Corneas, Dystrophy .
Endothelial Syndrome, Iridocorneal .
Endothelial Syndromes, Iridocorneal .
Iridocorneal Endothelial Syndromes .
A grouping of three closely linked conditions: iris nevus (or Cogan-Reese) syndrome, Chandler Syndrome, and essential (progressive) iris atrophy. The most common features of this syndrome are the movement of endothelial cells off the cornea onto the iris leading to corneal swelling, distortion of the iris, and variable degrees of distortion of the pupil. The abnormal cell movement plugs fluid outflow channels of the eye causing GLAUCOMA. .
Hyperaldosteronism .
Conn Syndrome .
Conn's Syndrome .
Primary Hyperaldosteronism .
Conns Syndrome .
Hyperaldosteronism, Primary .
Syndrome, Conn .
Syndrome, Conn's .
Aldosteronism .
A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. .