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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > disease > Disease of extremity > Congenital anomaly of limb > Congenital anomaly of digit (disorder) > Syndactyly (disorder) > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > Finding of limb structure > Disease of extremity > Congenital anomaly of limb > Congenital anomaly of digit (disorder) > Syndactyly (disorder) > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > disease > Congenital disease > Congenital malformation > Congenital anomaly of limb > Congenital anomaly of digit (disorder) > Syndactyly (disorder) > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
... > Clinical finding (finding) > disease > developmental disorder > Congenital malformation > Congenital anomaly of limb > Congenital anomaly of digit (disorder) > Syndactyly (disorder) > FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome

Preferred term

FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/774070008

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