{
    "disease_id": "DOID:0050725", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "keratosis palmoplantaris-corneal dystrophy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Tyrosinosis, oculocutaneous type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Richner-Hanhart syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosine transaminase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosine aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Oregon type tyrosinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "keratosis palmoplantaris with corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia, type II; TYRSN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Richner Hanhart syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia due to TAT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "TYRSN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "tyrosinemia due to tyrosine aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "oculocutaneous tyrosinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Tyrosinosis oculocutaneous type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010160", 
            "name": "Tat deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050725", 
            "name": "Oculocutaneous tyrosinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050725", 
            "name": "Richner-Hanhart syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050725", 
        "description": "A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050725", 
        "name": "tyrosinemia type II"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050725#disease-associations", 
            "id": "0050725", 
            "database": "Alliance of Genome Resources"
        }
    ]
}