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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)
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last database update
08/03/2022
MGI 6.21
The Jackson Laboratory