Disease association ontology term - MONDO:0010500 - intellectual disability, X-linked, syndromic 33

Term summary

ID

MONDO:0010500

Name

intellectual disability, X-linked, syndromic 33

Ontology or CV name

Disease association

Definition

Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the TAF1 gene.

Parents

• is_a congenital nervous system disorder
• is_a multiple congenital anomalies/dysmorphic syndrome-intellectual disability
• is_a X-linked syndromic intellectual disability

Annotation