Disease association ontology term - MONDO:0009627 - Galloway-Mowat syndrome

Term summary

ID

MONDO:0009627

Name

Galloway-Mowat syndrome

Ontology or CV name

Disease association

Definition

Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies.

Parents

• excluded_subClassOf syndromic intellectual disability
• is_a syndromic disease
• is_a autosomal recessive disease

Annotation