{
    "disease_id": "DOID:10908", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:10908", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:10908", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:10908", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:10908", 
            "name": "hydrocephalus, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "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.", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "Braddock Jones Superneau syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "hydrocephalus, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "HDCPH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "Braddock-Jones-Superneau syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007401", 
            "name": "hydrocephalus, autosomal dominant; HDCPH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "Any congenital hydrocephalus in which the cause of the disease is a mutation in the CCDC88C gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "hydrocephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "ventriculomegaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "CCDC88C congenital hydrocephalus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "HYC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "congenital hydrocephalus caused by mutation in CCDC88C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009360", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009360", 
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 1; HYC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "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.", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "X-linked hydrocephalus with stenosis of the aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "X-linked HSAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "hydrocephalus, X-linked, with congenital idiopathic intestinal pseudoobstruction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius; HSAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "X-linked acqueductal stenosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "HYCX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "HSAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "HSAS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "XLAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "hydrocephalus, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "X-linked hydrocephalus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "X-linked hydrocephalus with stenosis of aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "aqueductal stenosis, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "hydrocephalus with stenosis of the aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010611", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010611", 
            "name": "Bickers-Adams syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009361", 
            "name": "autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009361", 
            "name": "aqueductal stenosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009361", 
            "name": "hydrocephalus due to congenital stenosis of aqueduct of Sylvius"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014085", 
            "description": "Any congenital hydrocephalus in which the cause of the disease is a mutation in the MPDZ gene.", 
            "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 type 2"
        }, 
        {
            "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": "MPDZ congenital hydrocephalus"
        }, 
        {
            "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": "congenital hydrocephalus caused by mutation in MPDZ"
        }, 
        {
            "url": "https://www.omim.org/entry/236600", 
            "description": "Hydrocephalus, congenital, 1", 
            "resource": "MIM", 
            "id": "MIM:236600", 
            "name": "Hydrocephalus, congenital, 1"
        }, 
        {
            "url": "https://www.omim.org/entry/307000", 
            "description": "Hydrocephalus due to stenosis of the aqueduct of Sylvius", 
            "resource": "MIM", 
            "id": "MIM:307000", 
            "name": "Hydrocephalus due to stenosis of the aqueduct of Sylvius"
        }, 
        {
            "url": "https://www.omim.org/entry/615219", 
            "description": "Hydrocephalus, congenital, 2, with or without brain or eye anomalies", 
            "resource": "MIM", 
            "id": "MIM:615219", 
            "name": "Hydrocephalus, congenital, 2, with or without brain or eye anomalies"
        }
    ], 
    "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"
    }
}