{
    "disease_id": "DOID:0111669", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "juvenile hyaline fibromatosis (former subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "HFS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "infantile systemic hyalinosis (former subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "hyaline fibromatosis syndrome; HFS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "hyalinosis, systemic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009229", 
            "name": "inherited systemic hyalinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111669", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111669", 
            "name": "HFS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111669", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111669", 
            "name": "inherited systemic hyalinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111669", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111669", 
            "name": "puretic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111669", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111669", 
            "name": "systemic hyalinosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111669", 
        "description": "A connective tissue disease characterized by abnormal growth of hyalinized fibrous tissue especially around the subcutaneous regions on the scalp, ears, neck, face, hands, and feet, gingival hypertrophy, joint contractures, and osteolytic bone lesions that has_material_basis_in homozygous or compound heterozygous mutation in ANTXR2 on chromosome 4q21.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111669", 
        "name": "hyaline fibromatosis syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/228600", 
            "id": "228600", 
            "database": "MIM"
        }
    ]
}