{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "neonatal multiple carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "early-onset multiple carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "HLCS deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "multiple carboxylase deficiency, early onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "multiple carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "multiple carboxylase deficiency, neonatal form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "multiple carboxylase deficiency - neonatal onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "biotin-(propionyl-CoA-carboxylase) ligase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009666", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009666", 
            "name": "holocarboxylase synthase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:859", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:859", 
            "name": "Multiple carboxylase deficiency - neonatal onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:859", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:859", 
            "name": "Biotin-(propionyl-CoA-carboxylase) ligase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:859", 
        "description": "A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase.", 
        "resource": "Disease Ontology", 
        "id": "DOID:859", 
        "name": "holocarboxylase synthetase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/253270", 
            "id": "253270", 
            "database": "MIM"
        }
    ]
}