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Concept information

disease > genetic disease > hereditary disease > Simpson-Golabi-Behmel syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > pituitary diseases > gigantism > Simpson-Golabi-Behmel syndrome
disease > endocrinopathy > pituitary diseases > gigantism > Simpson-Golabi-Behmel syndrome
disease > stomatology > dysmorphic facies > Simpson-Golabi-Behmel syndrome
... > disease > congenital disease > malformation > dysmorphia > dysmorphic facies > Simpson-Golabi-Behmel syndrome
disease > congenital disease > malformation > macrosomia > Simpson-Golabi-Behmel syndrome
disease > pregnancy disease > fetal diseases > macrosomia > Simpson-Golabi-Behmel syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > pituitary diseases > overgrowth syndrome > Simpson-Golabi-Behmel syndrome
disease > endocrinopathy > pituitary diseases > overgrowth syndrome > Simpson-Golabi-Behmel syndrome
disease > diseases of the osteoarticular system > overgrowth syndrome > Simpson-Golabi-Behmel syndrome
disease > complex syndrome > overgrowth syndrome > Simpson-Golabi-Behmel syndrome

Preferred term

Simpson-Golabi-Behmel syndrome  

Definition(s)

  • Simpson–Golabi–Behmel syndrome (SGBS), is a rare inherited congenital disorder that can cause craniofacial, skeletal, cardiac, and renal abnormalities. (Wikipedia)

Broader concept(s)

Synonym(s)

  • Simpson dysmorphia syndrome

In other languages

URI

http://data.loterre.fr/ark:/67375/VH8-S6VW9FXT-P

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