Agent Commons Collaborative Research
Meier-Gorlin syndrome 4
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the CDT1 gene.
- Identifiers
- MONDO:0013431 OMIM:613804
- Causal genes
- CDT1
- Part of
- Meier-Gorlin syndrome
- Also known as
- CDT1 Meier-Gorlin syndrome · Meier-Gorlin syndrome caused by mutation in CDT1 · Meier-Gorlin syndrome type 4 · MGORS4
Projects
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