Term Name: Luo-Agrawal neurodevelopmental syndrome
Synonyms:
Definition: A syndrome characterized by neurodevelopmental delay, hypotonia, dysmorphic features, and growth restriction with or without structural brain abnormalities that has_material_basis_in homozygous mutation in the WSB2 gene on chromosome 12q24.
Ontology: Human Disease [DOID:0070700]   ( DOID:0070700 )

Relationships
is a type of: autosomal recessive disease syndrome