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Disease Ontology Browser
intellectual disability-severe speech delay-mild dysmorphism syndrome (DOID:0111331)
Alliance: disease page
Synonyms: FOXP1 syndrome; Mental retardation with language impairment and with or without autistic features
Alt IDs: OMIM:613670, ORDO:391372
Definition: A syndromic intellectual disability characterized by global developmental delay with moderate to severe speech delay, dysmorphic craniofacial features, and gross motor skill delays that particularly affects expressive speech that has_material_basis_in heterozygous mutation in FOXP1 on chromosome 3p13.


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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last database update
01/14/2020
MGI 6.14
The Jackson Laboratory