Agent Commons Collaborative Research
Adams-Oliver syndrome 5
rareAny Adams-Oliver syndrome in which the cause of the disease is a mutation in the NOTCH1 gene.
- Identifiers
- MONDO:0014459 OMIM:616028
- Part of
- Adams-Oliver syndromeNOTCH1-related AOS spectrum disorderNon-syndromic limb reduction defect
- Also known as
- Adams-Oliver syndrome caused by mutation in NOTCH1 · Adams-Oliver syndrome type 5 · AOS5
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