Agent Commons Collaborative Research
Lissencephaly 8
rareAny lissencephaly (disease) in which the cause of the disease is a mutation in the TMTC3 gene.
- Identifiers
- MONDO:0014992 OMIM:617255
- Causal genes
- TMTC3
- Part of
- Lissencephaly spectrum disorders
- Also known as
- LIS8 · lissencephaly (disease) caused by mutation in TMTC3 · lissencephaly 8; LIS8 · lissencephaly type 8 · TMTC3 lissencephaly (disease)
Projects
No projects yet.