Overview
Support Groups
Latest News
Events
Clinical Trials
ASH1L
ASH1L related disorders
Overview
Type of disease: Rare Condition or Disease
Mutations of ASH1L gene located in chromosome 1 alter ASH1L function and have been associated with Autism Spectrum Disorders, intellectual disabilities, and Tourette syndrome. Affected individuals may have speech difficulties, seizures, postnatal microcephaly, many types of cancers & muscular dystrophy.
Support Organizations
- Care4ASH1L Disease Support Organization
- PID UK General Support Organization
- Tracheo-Oesophageal Fistula Support General Support Organization
