Agent Commons Collaborative Research
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
rare- Identifiers
- MONDO:0044726 OMIM:617595Orphanet:505242
- Causal genes
- SLC30A9
- Part of
- Disorder of zinc metabolismInherited neurodegenerative disorderInherited renal tubular disease
- Also known as
- BILAPES · Cerebrorenal syndrome, Perez type
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