{
    "disease_id": "DOID:0070007", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel syndrome caused by mutation in ATR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "SCKL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Sckl"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "nanocephalic dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Bird-headed dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "microcephalic primordial dwarfism 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "microcephalic primordial dwarfism I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel-type dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "ATR Seckel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel syndrome 1; SCKL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel syndrome 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070007", 
            "name": "SCKL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070007", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070007", 
            "name": "microcephalic primordial dwarfism I"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070007", 
        "description": "A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070007", 
        "name": "Seckel syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070007#disease-associations", 
            "id": "0070007", 
            "database": "Alliance of Genome Resources"
        }
    ]
}