{
    "disease_id": "DOID:0070134", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "autosomal recessive cutis laxa type 2, classic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ARCL2, classic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ARCL2, Debr type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "Arcl2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa with Joint laxity and retarded development"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa, autosomal recessive, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa, autosomal recessive, type IIA; ARCL2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa with congenital disorder of glycosylation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ARCL2, debre type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ADCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ARCL2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa, autosomal recessive, type IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa with Growth and developmental delay"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa, autosomal recessive type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "ARCL2, DebrC) type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "autosomal recessive cutis laxa type 2, DebrC) type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "autosomal recessive cutis laxa type II classic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa with bone dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "cutis laxa, debre type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009054", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009054", 
            "name": "autosomal recessive cutis laxa type 2, Debr type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070134", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070134", 
            "name": "ARCL2A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070134", 
        "description": "An autosomal recessive cutis laxa type II classic type that has_material_basis_in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070134", 
        "name": "autosomal recessive cutis laxa type IIA"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=23545", 
            "id": "23545", 
            "database": "GlyCosmos"
        }
    ]
}