{
    "disease_id": "DOID:0050569", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008869", 
            "name": "Seckel syndrome 1"
        }, 
        {
            "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:0050569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050569", 
            "name": "Harper's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050569", 
            "name": "Virchow-Seckel dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050569", 
            "name": "bird-headed dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050569", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050569", 
            "name": "microcephalic primordial dwarfism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050569", 
        "description": "A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050569", 
        "name": "Seckel syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050569#disease-associations", 
            "id": "0050569", 
            "database": "Alliance of Genome Resources"
        }
    ]
}