{
    "disease_id": "DOID:10908", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 2; HYC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "HYC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "MPDZ congenital hydrocephalus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "congenital hydrocephalus caused by mutation in MPDZ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014085", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:10908", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:10908", 
            "name": "hydrocephalus, X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:10908", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:10908", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:10908", 
        "description": "A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head.", 
        "resource": "Disease Ontology", 
        "id": "DOID:10908", 
        "name": "hydrocephalus"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/10908#disease-associations", 
            "id": "10908", 
            "database": "Alliance of Genome Resources"
        }
    ]
}