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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
- Children’s Alopecia Project, Inc. General Support Organization
- Retina UK General Support Organization
- Care4ASH1L Disease Support Organization
