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Disease Ontology Browser
acrocallosal syndrome (DOID:9250)
Alliance: disease page
Synonyms: ACLS; SCHINZEL ACROCALLOSAL SYNDROME; Schinzel syndrome 1
Alt IDs: OMIM:200990, MESH:D055673, NCI:C84531, UMLS_CUI:C0796147
Definition: A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation.

Disease References using Mouse Models (1)
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
11/12/2024
MGI 6.24 		The Jackson Laboratory