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Disease Ontology Browser
Mulvihill-Smith syndrome (DOID:0061154)
Alliance: disease page
Synonyms: progeroid short stature with pigmented nevi
Alt IDs: OMIM:176690, ORDO:2959
Definition: A progeroid syndrome that is characterized by premature aging, multiple pigmented nevi, lack of facial subcutaneous fat, microcephaly, short stature, sensorineural hearing loss, and impaired intellectual development.

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
03/18/2025
MGI 6.24 		The Jackson Laboratory