{
    "disease_id": "DOID:0050778", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel syndrome, type 1; MKS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel-Gruber syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "MKS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "MKS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "MKS1 Meckel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel Gruber syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Gruber syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Mes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel syndrome type1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Dysencephalia Splanchnocystica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel syndrome caused by mutation in MKS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Meckel-Gruber syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009571", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009571", 
            "name": "Dysencephalia splachnocystica"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050778", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050778", 
            "name": "Meckel-Gruber syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050778", 
        "description": "A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050778", 
        "name": "Meckel syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050778#disease-associations", 
            "id": "0050778", 
            "database": "Alliance of Genome Resources"
        }
    ]
}