autosomal recessive intellectual developmental disorder 66 Disease Ontology Browser

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autosomal recessive intellectual developmental disorder 66 (DOID:0081227)
Alliance: disease page
Alt IDs: OMIM:618221
Definition: An autosomal recessive intellectual developmental disorder that is characterized by delayed speech development, neuropsychiatric symptoms, and relatively normal life span and that has_material_basis_in homozygous mutation in the C12ORF4 gene on chromosome 12p13.

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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