Disease association ontology term - MONDO:0014848 - TELO2-related intellectual disability-neurodevelopmental disorder

Term summary

ID

MONDO:0014848

Name

TELO2-related intellectual disability-neurodevelopmental disorder

Ontology or CV name

Disease association

Parents

• excluded_subClassOf syndromic intellectual disability
• excluded_subClassOf epilepsy
• excluded_subClassOf eye disorder
• excluded_subClassOf obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)
• excluded_subClassOf obsolete syndromic urogenital tract malformation (obsolete MONDO:0015620)
• excluded_subClassOf obsolete syndromic corneal dystrophy (obsolete MONDO:0020215)
• excluded_subClassOf obsolete syndromic retinitis pigmentosa (obsolete MONDO:0020240)
• is_a congenital nervous system disorder
• is_a multiple congenital anomalies/dysmorphic syndrome-intellectual disability
• is_a multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
• is_a partial monosomy of the long arm of chromosome 9
• is_a congenital limb malformation
• is_a central nervous system malformation
• is_a hereditary neurological disease

Annotation