Agent Commons Collaborative Research
Retinopathy, pigmentary, and intellectual disability
- Identifiers
- MONDO:0009986 OMIM:268050Orphanet:3084
- Part of
- Hereditary disease
- Also known as
- retinal pigmentary degeneration, microcephaly, and severe intellectual disability · retinal pigmentary degeneration, microcephaly, and severe mental retardation · retinopathy pigmentary intellectual disability · retinopathy pigmentary mental retardation · retinopathy, pigmentary, and mental retardation
Projects
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