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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
... > Clinical finding (finding) > disease > Disease of head > Congenital anomaly of head > Congenital anomaly of eye > Microphthalmos > Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Congenital anomaly of head > Congenital anomaly of eye > Microphthalmos > Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
... > Clinical finding (finding) > disease > Congenital disease > Congenital malformation > Congenital anomaly of head > Congenital anomaly of eye > Microphthalmos > Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
... > Clinical finding (finding) > disease > developmental disorder > Congenital malformation > Congenital anomaly of head > Congenital anomaly of eye > Microphthalmos > Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)

Preferred term

Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)  

Type

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

Associated morphology

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/718761007

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