{
    "disease_id": "DOID:10908",
    "recommended_name": {
        "id": "DOID:10908",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:10908",
        "name": "hydrocephalus",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:10908",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10908",
            "name": "hydrocephalus, X-linked",
            "description": ""
        },
        {
            "id": "DOID:10908",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10908",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome",
            "description": "Craniosynostosis, Dandy-Walker malformation and hydrocephalus is a malformation disorder characterized by sagittal craniosynostosis (see this term), Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. The inheritance pattern appears to be autosomal dominant."
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "HDCPH1",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "Braddock Jones Superneau syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "hydrocephalus, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "hydrocephalus, autosomal dominant; HDCPH1",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007401",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007401",
            "name": "Braddock-Jones-Superneau syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1",
            "description": "Any congenital hydrocephalus in which the cause of the disease is a mutation in the CCDC88C gene."
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "CCDC88C congenital hydrocephalus",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1; HYC1",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "HYC1",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "hydrocephaly",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "ventriculomegaly",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "congenital hydrocephalus caused by mutation in CCDC88C",
            "description": ""
        },
        {
            "id": "MONDO:0009360",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009360",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "X-linked hydrocephalus with stenosis of the aqueduct of Sylvius",
            "description": "A form of L1 syndrome caused by changes in the L1CAM gene characterized by severe hydrocephalus mostly with prenatal onset, signs of intracranial hypertension, adducted thumbs, spasticity, and severe intellectual deficit. HSAS represents the severe end of the spectrum and is associated with poor prognosis."
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "hydrocephalus, X-linked, with congenital idiopathic intestinal pseudoobstruction",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius; HSAS",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "HYCX",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "XLAS",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "aqueductal stenosis, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "Bickers-Adams syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "X-linked hydrocephalus",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "HSAS",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "X-linked hydrocephalus with stenosis of aqueduct of Sylvius",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "hydrocephalus, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "X-linked HSAS",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "hydrocephalus with stenosis of the aqueduct of Sylvius",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "X-linked acqueductal stenosis",
            "description": ""
        },
        {
            "id": "MONDO:0010611",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010611",
            "name": "HSAS1",
            "description": ""
        },
        {
            "id": "MONDO:0009361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009361",
            "name": "autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius",
            "description": ""
        },
        {
            "id": "MONDO:0009361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009361",
            "name": "aqueductal stenosis",
            "description": ""
        },
        {
            "id": "MONDO:0009361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009361",
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 2",
            "description": "Any congenital hydrocephalus in which the cause of the disease is a mutation in the MPDZ gene."
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 2; HYC2",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "HYC2",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "MPDZ congenital hydrocephalus",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 2",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "congenital hydrocephalus caused by mutation in MPDZ",
            "description": ""
        },
        {
            "id": "MONDO:0014085",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014085",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive type 2",
            "description": ""
        },
        {
            "id": "MIM:236600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/236600",
            "name": "Hydrocephalus, congenital, 1",
            "description": "Hydrocephalus, congenital, 1"
        },
        {
            "id": "MIM:307000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/307000",
            "name": "Hydrocephalus due to stenosis of the aqueduct of Sylvius",
            "description": "Hydrocephalus due to stenosis of the aqueduct of Sylvius"
        },
        {
            "id": "MIM:615219",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615219",
            "name": "Hydrocephalus, congenital, 2, with or without brain or eye anomalies",
            "description": "Hydrocephalus, congenital, 2, with or without brain or eye anomalies"
        }
    ]
}