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Disease Ontology Browser
Wiedemann-Rautenstrauch syndrome (DOID:0081333)
Alliance: disease page
Synonyms: Neonatal progeroid syndrome; PROGEROID SYNDROME, NEONATAL
Alt IDs: OMIM:264090, ORDO:3455
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory