{
    "disease_id": "DOID:0050475", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "glaucoma-ectopia-microspherophakia-stiff joints-short stature syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "mesodermal Dysmorphodystrophy, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "Weill-Marchesani syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "GEMSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "Weill-Marchesani syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "spherophakia-brachymorphia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "WMS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "Weill-Marchesani syndrome 2; WMS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "GEMSS syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012013", 
            "name": "Weill-Marchesani syndrome, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050475", 
            "name": "GEMSS syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050475", 
            "name": "Marchesani-Weill Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050475", 
            "name": "Mesodermal Dysmorphodystrophy, Congenital"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050475", 
            "name": "Spherophakia Brachymorphia Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050475", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050475", 
            "name": "congenital mesodermal dystrophy"
        }, 
        {
            "url": "https://www.omim.org/entry/608328", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608328", 
            "name": "Weill-Marchesani syndrome 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050475", 
        "description": "A syndrome characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050475", 
        "name": "Weill-Marchesani syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608328", 
            "id": "608328", 
            "database": "MIM"
        }
    ]
}