{
    "disease_id": "DOID:0070137", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "autosomal recessive cutis laxa type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "cutis laxa, autosomal recessive, type IIB; ARCL2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "cutis laxa, autosomal recessive, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "PYCR1 autosomal recessive cutis laxa type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "cutis laxa with progeroid features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "cutis laxa, autosomal recessive, type IIB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "autosomal recessive cutis laxa type 2, progeroid type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "autosomal recessive cutis laxa type 2 caused by mutation in PYCR1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "ARCL2, progeroid type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "cutis laxa, autosomal recessive type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013051", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013051", 
            "name": "ARCL2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070137", 
            "name": "ARCL2, progeroid type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070137", 
            "name": "ARCL2B"
        }, 
        {
            "url": "https://www.omim.org/entry/612940", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612940", 
            "name": "Cutis laxa, autosomal recessive, 2B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070137", 
        "description": "A cutis laxa characterized by progeroid features that has_material_basis_in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070137", 
        "name": "autosomal recessive cutis laxa type IIB"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612940", 
            "id": "612940", 
            "database": "MIM"
        }
    ]
}