Term Name: pontocerebellar hypoplasia type 2D
Synonyms:
Definition: A pontocerebellar hypoplasia that is characterized by progressive microcephaly, profound intellectual disability, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the SEPSECS gene.
Ontology: Human Disease [DOID:0060270]   ( DOID:0060270 )

Relationships
is a type of: autosomal recessive disease pontocerebellar hypoplasia type 2