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 Jagell Holmgren Hofer syndrome
C537364
 
  
  
  


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C11. Eye Diseases: Eye Diseases [MESH:D005128] > Eyelid Diseases [MESH:D005141] > Ectropion [MESH:D004483]
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A. Anatomy 
A. Anatomy
 Body Regions [MESH:D001829] (867) 
 Head [MESH:D006257] (523) 
 Face [MESH:D005145] (387) 
 Mouth [MESH:D009055] (40) 
 Lip [MESH:D008046] (39) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Stomatognathic System [MESH:D013284] (673) 
 Mouth [MESH:D009055] (194) 
 Lip [MESH:D008046] (42) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C07. Stomatognathic Diseases 
C07. Stomatognathic Diseases
 Stomatognathic Diseases [MESH:D009057] (5348) 
 Mouth Diseases [MESH:D009059] (4783) 
 Mouth Abnormalities [MESH:D009056] (1383) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Mouth Abnormalities [MESH:D009056] (1383) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C10. Nervous System Diseases 
C10. Nervous System Diseases
 Nervous System Diseases [MESH:D009422] (13325) 
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Intellectual Disability [MESH:D008607] (3054) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C11. Eye Diseases 
C11. Eye Diseases
 Eye Diseases [MESH:D005128] (6245) 
 Eyelid Diseases [MESH:D005141] (882) 
 Ectropion [MESH:D004483] (5) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
 Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) 
 Congenital Abnormalities [MESH:D000013] (8109) 
 Skin Abnormalities [MESH:D012868] (1723) 
 Ichthyosis [MESH:D007057] (481) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Mouth Abnormalities [MESH:D009056] (1383) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Ichthyosis [MESH:D007057] (476) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Skin Diseases [MESH:D012871] (8774) 
 Hair Diseases [MESH:D006201] (1891) 
 Hypotrichosis [MESH:D007039] (1513) 
 Alopecia [MESH:D000505] (1453) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Keratosis [MESH:D007642] (1941) 
 Ichthyosis [MESH:D007057] (481) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Skin Abnormalities [MESH:D012868] (1709) 
 Ichthyosis [MESH:D007057] (481) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Signs and Symptoms [MESH:D012816] (10659) 
 Neurologic Manifestations [MESH:D009461] (8702) 
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Intellectual Disability [MESH:D008607] (1476) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
F. Psychiatry and Psychology 
F. Psychiatry and Psychology
 Behavior and Behavior Mechanisms [MESH:D001520] (1594) 
 Neurobehavioral Manifestations [MESH:D019954] (1206) 
 Intellectual Disability [MESH:D008607] (1109) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)
 Mental Disorders [MESH:D001523] (2063) 
 Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245) 
 Intellectual Disability [MESH:D008607] (1109) 
 Jagell Holmgren Hofer syndrome [MESH:C537364] (1)