skip to main content

Content language

Contact us: CRM@email.irandoc.ac.ir

Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies

Preferred term

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies  

Type

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

Associated morphology

Finding site

URI

http://www.irandoc.acir/onto/irandoc/774152007

Download this concept: