{
    "disease_id": "DOID:0111331", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111331", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111331", 
            "name": "FOXP1 syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111331", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111331", 
            "name": "Mental retardation with language impairment and with or without autistic features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "Intellectual disability-severe speech delay-mild dysmorphism syndrome, also known as intellectual disability with language impairment and with or without autistic features, is adisorder characterized by global developmental delay with moderate to severe speech delay thataffects expressive speech. Most patients have difficulty articulating words. Common signs and symptoms include broad forehead, downslanting palpebral fissures, short nose with broad tip, head appearing too large for the body, frontal hair upsweep, and bulging digit pads anddelatyed gross motor skills. Some patients have autistic features and/or behavioral problems. Congenital malformations may be associated. All reported cases have occurred de novo (without any cases in the family). It is caused by alterations (mutations) in the caused by heterozygous mutation in the FOXP1 gene .", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "intellectual disability-severe speech delay-mild dysmorphism syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "FOXP1 related global developmental delay, intellectual disability and speech defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "mental retardation with language impairment and with or without autistic features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "intellectual disability with language impairment and with or without autistic features"
        }, 
        {
            "url": "https://www.omim.org/entry/613670", 
            "description": "Mental retardation with language impairment and autistic features", 
            "resource": "MIM", 
            "id": "MIM:613670", 
            "name": "Mental retardation with language impairment and autistic features"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111331", 
        "description": "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111331", 
        "name": "intellectual disability-severe speech delay-mild dysmorphism syndrome"
    }
}