{
    "disease_id": "DOID:0111873", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "trichothiodystrophy 1, photosensitive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "TTD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "Tay syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "PIBIDS syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "trichothiodystrophy with congenital ichthyosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "trichothiodystrophy 1, photosensitive; TTD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "trichothiodystrophy, photosensitive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011125", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011125", 
            "name": "ichthyosiform erythroderma with hair Abnormality and mental and Growth retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111873", 
            "name": "TTD1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111873", 
        "description": "A photosensitive trichothiodystrophy that has_material_basis_in homozygous or compound heterozygous mutation in ERCC2  on chromosome 19q13.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111873", 
        "name": "photosensitive trichothiodystrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111873#disease-associations", 
            "id": "0111873", 
            "database": "Alliance of Genome Resources"
        }
    ]
}