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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.

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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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11/12/2024
MGI 6.24 		The Jackson Laboratory