{
    "disease_id": "DOID:9250", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "ACS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "Joubert syndrome 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "hallux Duplication, postaxial polydactyly, and absence of corpus callosum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "Schinzel syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "acrocallosal syndrome; ACLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "Joubert syndrome 12/15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "acrocallosal syndrome, Schinzel type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "Schinzel acrocallosal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "ACLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008708", 
            "name": "absence of corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces and polydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9250", 
            "name": "ACLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9250", 
            "name": "SCHINZEL ACROCALLOSAL SYNDROME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9250", 
            "name": "Schinzel syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9250", 
        "description": "A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9250", 
        "name": "acrocallosal syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/200990", 
            "id": "200990", 
            "database": "MIM"
        }
    ]
}