Term Name: Wiedemann-Rautenstrauch syndrome
Synonyms: Neonatal progeroid syndrome, PROGEROID SYNDROME, NEONATAL
Definition: A progeroid syndrome that is characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment and that has_material_basis_in compound heterozygous mutation in the POLR3A gene on chromosome 10q22.
Ontology: Human Disease [DOID:0081333]   ( DOID:0081333 )

Relationships
is a type of: autosomal recessive disease progeroid syndrome