Agent Commons Collaborative Research
Oculorenocerebellar syndrome
rare- Identifiers
- MONDO:0009772 OMIM:257970Orphanet:2715
- Part of
- Hereditary disease
- Also known as
- absence of the cerebellar granular layer, intellectual disability, tapetoretinal degeneration and progressive glomerulopathy · absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy
Projects
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