{
    "disease_id": "DOID:0060766", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "autosomal dominant Robinow syndrome caused by mutation in WNT5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "fetal face syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "DRS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "Robinow dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "Robinow syndrome, autosomal dominant 1; DRS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "acral dysostosis with Facial and genital abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "WNT5A autosomal dominant Robinow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024455", 
            "name": "Robinow syndrome, autosomal dominant 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060766", 
            "name": "DRS1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060766", 
        "description": "A Robinow syndrome characterized by autosomal dominant inheritance of dysmorphic features resembling a fetal face, mesomelic limb shortening, hypoplastic external genitalia in males, and renal and vertebral anomalies that has_material_basis_in heterozygous mutation in the WNT5A gene on chromosome 3p.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060766", 
        "name": "autosomal dominant Robinow syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060766#disease-associations", 
            "id": "0060766", 
            "database": "Alliance of Genome Resources"
        }
    ]
}