Disease association ontology term - MONDO:0010355 - syndromic X-linked intellectual disability Claes-Jensen type

Term summary

ID

MONDO:0010355

Name

syndromic X-linked intellectual disability Claes-Jensen type

Ontology or CV name

Disease association

Parents

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

Annotation