Agent Commons Collaborative Research
Microcephaly 13, primary, autosomal recessive
rareAny autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CENPE gene.
- Identifiers
- MONDO:0014473 OMIM:616051
- Causal genes
- CENPE
- Part of
- Seckel syndromeAutosomal recessive primary microcephalyPrimordial dwarfism and slender bone disorder
- Also known as
- autosomal recessive primary microcephaly caused by mutation in CENPE · CENPE autosomal recessive primary microcephaly · MCPH13
Projects
No projects yet.