About   Help   FAQ
Disease Ontology Browser
Robinow syndrome (DOID:0060254)
Alliance: disease page
Synonyms: acral dysostosis with facial and genital abnormalities; fetal face syndrome; Robinow dwarfism
Alt IDs: ICD10CM:Q87.19, MESH:C562492, NCI:C85048, OMIM:PS268310, ORDO:97360, UMLS_CUI:C0265205
Definition: A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities.

Disease References using Mouse Models (4)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
03/18/2025
MGI 6.24 		The Jackson Laboratory