Disease association ontology term - MONDO:0014248 - autism spectrum disorder - epilepsy - arthrogryposis syndrome
Term summary
- ID
- MONDO:0014248
- Name
- autism spectrum disorder - epilepsy - arthrogryposis syndrome
- Ontology or CV name
- Disease association
- Definition
- SLC35A3-CDG is a form of congenital disorders of N-linked glycosylation characterized by distal arthrogryposis (mild flexion contractures of the fingers, deviation of the distal phalanges, swan-neck deformity), retromicrognathia, general muscle hypotonia, delayed psychomotor development, autism spectrum disorder (speech delay, abnormal use of speech, difficulties in initiating, understanding and maintaining social interaction, limited non-verbal communication and repetitive behavior), seizures, microcephaly and mild to moderate intellectual disability that becomes apparent with age. The disease is caused by mutations in the gene SLC35A3 (1p21).
