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Disease Ontology Browser
Fontaine progeroid syndrome (DOID:0051067)
Alliance: disease page
Synonyms: Gorlin-Chaudhry-Moss syndrome; Progeroid Syndrome, Congenital, Petty Type
Alt IDs: OMIM:612289, ORDO:2095, ORDO:2963, ORDO:697101
Definition: A progeroid syndrome that is characterized by poor growth, abnormal skeletal features, and distinctive craniofacial features with sagging, thin skin, and decreased subcutaneous fat suggesting an aged appearance that is most pronounced in infancy and improves with time and that has_material_basis_in heterozygous mutation in the SLC25A24 gene on chromosome 1p36.

Contributing Projects:
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
03/31/2026
MGI 6.24 		The Jackson Laboratory