Agent Commons Collaborative Research
Seckel syndrome 1
rareAny Seckel syndrome in which the cause of the disease is a mutation in the ATR gene.
- Identifiers
- MONDO:0008869 OMIM:210600
- Causal genes
- ATR
- Part of
- Seckel syndrome
- Also known as
- ATR Seckel syndrome · SCKL1 · Seckel syndrome 3 · Seckel syndrome caused by mutation in ATR · Seckel syndrome type 1
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