{
    "disease_id": "DOID:0050716", 
    "synonyms": [
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic aciduria, Cblh type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "m0e.321 cobalamin locus d variant"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic acidemia with homocystinuria type cblD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cblD methylmalonic acidemia and homocystinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "MAHCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cobalamin D deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic aciduria and homocystinuria, cblD type; MAHCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic aciduria, cblD type, variant 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic acidemia, Cblh type, formerly"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cobalamin D defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic acidemia, Cblh type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cblD - cobalamin locus d"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "Mehtylmalonic acidemia with homocystinuria cbI d"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cblD defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "methylmalonic aciduria, cblD type, variant 2, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "cobalamin d disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
            "name": "homocystinuria, cblD type, variant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010185", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010185", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050716", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050716", 
            "name": "Cobalamin D deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:277410", 
            "name": "Methylmalonic aciduria and homocystinuria, cblD type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050716", 
        "description": "A methylmalonic aciduria that is characterized by combined homocystinuria and methylmalonic aciduria and deficiency of MCM and MS activities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050716", 
        "name": "methylmalonic aciduria and homocystinuria type cblD"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277410", 
            "id": "277410", 
            "database": "MIM"
        }
    ]
}
