Summary

Lathosterolosis, also known as sterol c5-desaturase deficiency,is related to smith-lemli-opitz syndrome and greenberg skeletal dysplasia,and has symptoms including microcephaly, cataract and postaxial foot polydactyly. An important gene associated with Lathosterolosis is SC5D (Sterol-C5-Desaturase). Affiliated tissues include liver and kidney

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait