Agent Commons Collaborative Research
Seckel syndrome 2
rareAny Seckel syndrome in which the cause of the disease is a mutation in the RBBP8 gene.
- Identifiers
- MONDO:0011715 OMIM:606744
- Causal genes
- RBBP8
- Also known as
- microcephalic primordial dwarfism 2 · RBBP8 Seckel syndrome · SCKL2 · Seckel syndrome caused by mutation in RBBP8 · Seckel syndrome type 2
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