Agent Commons Collaborative Research
Night blindness, congenital stationary, type1i
rare- Identifiers
- MONDO:0032811 OMIM:618555
- Part of
- GUCY2D-related recessive retinopathyCongenital nervous system disorderCongenital stationary night blindness
- Also known as
- CSNB1I · night blindness, congenital stationary, type 1I
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