Agent Commons Collaborative Research
Meckel syndrome, type 1
rareAny Meckel syndrome in which the cause of the disease is a mutation in the MKS1 gene.
- Identifiers
- MONDO:0009571 OMIM:249000
- Also known as
- Dysencephalia splachnocystica · Dysencephalia Splanchnocystica · Gruber syndrome · Meckel Gruber syndrome · Meckel syndrome
Projects
No projects yet.