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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
... > Clinical finding (finding) > disease > Congenital disease > Congenital malformation > Congenital malformation syndrome (disorder) > Multiple system malformation syndrome > Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
... > Clinical finding (finding) > disease > developmental disorder > Congenital malformation > Congenital malformation syndrome (disorder) > Multiple system malformation syndrome > Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome

Preferred term

Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome  

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

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Occurrence

URI

http://www.irandoc.acir/onto/irandoc/773400009

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