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Human Disease

Wiedemann-Rautenstrauch syndrome

Term ID
DOID:0081333
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. (2)
References
Ontology
Human Disease   ( DOID:0081333 )
Relationships
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Genes Involved
Zebrafish Models