{
    "disease_id": "DOID:0111822",
    "recommended_name": {
        "id": "DOID:0111822",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111822",
        "name": "CHILD syndrome",
        "description": "A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in the NSDHL gene on chromosome Xq28."
    },
    "synonyms": [
        {
            "id": "DOID:0111822",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111822",
            "name": "CHILD nevus",
            "description": ""
        },
        {
            "id": "DOID:0111822",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111822",
            "name": "congenital hemidysplasia with ichthyosiform nevus and limbs defects",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "CHILD syndrome",
            "description": "CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies."
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "CHILD syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "CHILD syndrome, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "Ichthyosis, CHILD Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "child nevus",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "child syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "congenital hemidysplasia with ichthyosiform nevus and limb defects",
            "description": ""
        },
        {
            "id": "MONDO:0010621",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010621",
            "name": "ichthyosis, child syndrome",
            "description": ""
        },
        {
            "id": "MIM:308050",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/308050",
            "name": "Congenital hemidysplasia with ichthyosiform erythroderma and limb defects",
            "description": "Congenital hemidysplasia with ichthyosiform erythroderma and limb defects"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111822"
    ],
    "unlinked_id_list": []
}