Disease association ontology term - MONDO:0007988 - autosomal dominant primary microcephaly

Term summary

ID

MONDO:0007988

Name

autosomal dominant primary microcephaly

Ontology or CV name

Disease association

Definition

Autosomal dominant form of microcephaly (disease).

Parents

• is_a autosomal dominant disease
• is_a congenital nervous system disorder
• is_a multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
• is_a isolated congenital microcephaly
• is_a Mendelian neurodevelopmental disorder

Annotation