{
    "disease_id": "DOID:0070132", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070132", 
            "name": "ARCL3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070132", 
            "name": "De Barsy syndrome A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "ALDH18A1-related De Barsy syndrome combines intellectual deficit, bilateral cataracts, and skin and joint hyperlaxity.", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "ALDH18A1-related de Barsy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "De Barsy syndrome A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "neurocutaneous syndrome, Bicknell type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "cutis laxa, autosomal recessive, type 3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "P5CS deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "cutis laxa, corneal clouding, and mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "Delta-1-pyrroline 5-carboxylate synthetase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "autosomal recessive cutis laxa type IIIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "ARCL3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "cutis laxa, autosomal recessive, type IIIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "cutis laxa, autosomal recessive, type IIIA; ARCL3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "De Barsy syndrome a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009053", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009053", 
            "name": "progeroid syndrome of De Barsy"
        }, 
        {
            "url": "https://www.omim.org/entry/219150", 
            "description": "Cutis laxa, autosomal recessive, 3A", 
            "resource": "MIM", 
            "id": "MIM:219150", 
            "name": "Cutis laxa, autosomal recessive, 3A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070132", 
        "description": "A autosomal recessive cutis laxa type III that has_material_basis_in homozygous mutation in the ALDH18A1 gene on chromosome 10q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070132", 
        "name": "autosomal recessive cutis laxa type IIIA"
    }
}