{
    "disease_id": "DOID:12960", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:12960", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12960", 
            "name": "Apert syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "Apert syndrome (AS) is a frequent form of acrocephalosyndactyly (see this term), a group of inherited congenital malformation disorders, characterized by craniosynostosis (see this term), midface hypoplasia, and finger and toe anomalies and/or syndactyly.", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "apert syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "apert-Crouzon disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "Vogt Cephalodactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "acrocephalosyndactyly type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "acrocephalosyndactyly, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "ACS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "type I Acrocephalosyndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "acrocephalosyndactyly, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "acrocephalosyndactyly type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "syndactylic oxycephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "acrocephalo-syndactyly type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "apert syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "ACS 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007041", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007041", 
            "name": "ACS 1"
        }, 
        {
            "url": "https://www.omim.org/entry/101200", 
            "description": "Apert syndrome", 
            "resource": "MIM", 
            "id": "MIM:101200", 
            "name": "Apert syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12960", 
        "description": "A synostosis that results_in craniosynostosis and syndactyly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:12960", 
        "name": "acrocephalosyndactylia"
    }
}