Chromosome 1p36 Deletion Syndrome

Chromosome 1p36 Deletion Syndrome, also known as 1p36 deletion syndrome, is related to chromosome 1p36 deletion syndrome, proximal and chromosome 1p36 deletion syndrome, distal, and has symptoms including seizures An important gene associated with Chromosome 1p36 Deletion Syndrome is SPEN (Spen Family Transcriptional Repressor), and among its related pathways/superpathways are 1p36 copy number variation syndrome and Thromboxane A2 receptor signaling. Affiliated tissues include heart and brain, and related phenotypes are intellectual disability and agenesis of corpus callosum