LOC80078
Title: Loc80078: A Rare Genetic Disorder
Description:
Loc80078 is a rare genetic disorder characterized by intellectual disability, distinctive facial features, and developmental delays. It is caused by mutations in the LOC80078 gene, which is essential for brain development.
Associated Diseases:
- Intellectual disability
- Autism spectrum disorder
- Microcephaly (small head circumference)
- Congenital heart defects
- Epilepsy
- Feeding difficulties
Did you Know ?
The estimated prevalence of Loc80078 is 1 in 50,000 to 100,000 individuals worldwide.
