{
    "disease_id": "DOID:0111668", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "amelocerebrohypohidrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "KTZS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "Kohlschutter Tonz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "epilepsy-dementia-amelogenesis imperfecta syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "epilepsy and Yellow teeth"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "KOHLSCHUTTER-Tonz syndrome; KTZS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "epilepsy, dementia, and amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "epilepsy dementia amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009185", 
            "name": "Kohlschutter syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "KTZS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "Kohlschutter's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "amelocerebrohypohidrotic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "epilepsy and yellow teeth"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "epilepsy dementia amelogenesis imperfecta"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111668", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111668", 
            "name": "epilepsy-dementia-amelogenesis imperfecta syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/226750", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:226750", 
            "name": "Kohlschuetter-Toenz syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111668", 
        "description": "A syndrome characterized by severe global developmental delay, early-onset intractable seizures, spasticity, and amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in ROGDI on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111668", 
        "name": "Kohlschutter-Tonz syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/226750", 
            "id": "226750", 
            "database": "MIM"
        }
    ]
}