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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Cerebral degeneration > Cerebral degeneration (disorder) > Cerebral atrophy > Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome

Preferred term

Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome  

Type

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

Associated morphology

Has interpretation

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/782757004

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