Term Name: neuronal ceroid lipofuscinosis 15
Synonyms:
Definition: A neuronal ceroid lipofuscinosis that is characterized by severe global developmental delay apparent in infancy or early childhood and that has_material_basis_in heterozygous mutation in the CLCN6 gene on chromosome 1p36.
Ontology: Human Disease [DOID:0061189]   ( DOID:0061189 )

Relationships
is a type of: autosomal dominant disease neuronal ceroid lipofuscinosis