About   Help   FAQ
Disease Ontology Browser
acrofacial dysostosis, Catania type (DOID:0060384)
Alliance: disease page
Synonyms: Opitz Mollica Sorge syndrome; Opitz-Caltabiano syndrome
Alt IDs: OMIM:101805, MESH:C538182, ORDO:1786, UMLS_CUI:C2931762
Definition: An acrofacial dysostosis that is characterized by intrauterine growth retardation, short stature, microcephaly, cleft palate, limb hypoplasia, simian creases and cryptorchidism/hypospadias.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory