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Disease Ontology Browser
autosomal dominant intellectual developmental disorder 56 (DOID:0080226)
Alliance: disease page
Synonyms: autosomal dominant intellectual developmental disorder-56; autosomal dominant mental retardation 56
Alt IDs: OMIM:617854
Definition: An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay, intellectual disability and in most cases hypotonia, delayed walking, poor fine motor skills, and poor or absent speech that has_material_basis_in heterozygous mutation in the CLTC gene on chromosome 17q23.

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