Summary

Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome, also known as jp/hht syndrome,is related to hereditary hemorrhagic telangiectasia and leukemia,and has symptoms including juvenile gastrointestinal polyposis, pulmonary arteriovenous malformation and clubbing. An important gene associated with Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome is SMAD4 (SMAD Family Member 4). Affiliated tissues include skin, lung and liver

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait