{
    "disease_id": "DOID:0060762",
    "recommended_name": {
        "id": "DOID:0060762",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060762",
        "name": "restrictive dermopathy",
        "description": "A skin disease characterized by thin, tightly adherent translucent skin with erosions at flexure sites, superficial vessels, typical facial dysmorphism, and generalized joint ankylosis. Prenatal signs may include intrauterine growth retardation, reduced fetal movements, polyhydramnios, and premature rupture of the membranes. Most infants die within the first week of life."
    },
    "synonyms": [
        {
            "id": "DOID:0060762",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060762",
            "name": "hyperkeratosis-contracture syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060762",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060762",
            "name": "tight skin contracture syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060762",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060762",
            "name": "lethal restrictive dermopathy",
            "description": ""
        },
        {
            "id": "DOID:0060762",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060762",
            "name": "Infantile restrictive dermopathy",
            "description": ""
        },
        {
            "id": "DOID:0060762",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060762",
            "name": "Lethal tight skin contracture syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "restrictive dermopathy 1",
            "description": "A restrictive dermopathy that has material basis in homozygous or compound heterozygous mutation in the ZMPSTE24 gene on chromosome 1p34."
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "restrictive dermopathy",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "fetal hypokinesia sequence due to restrictive dermopathy",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "foetal hypokinesia sequence due to restrictive dermopathy",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "hyperkeratosis-contracture syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "restrictive dermopathy 1, lethal",
            "description": ""
        },
        {
            "id": "MONDO:0800042",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800042",
            "name": "tight skin contracture syndrome, lethal",
            "description": ""
        },
        {
            "id": "MIM:275210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/275210",
            "name": "Restrictive dermopathy 1",
            "description": "Restrictive dermopathy 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0070369",
            "label": "restrictive dermopathy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070370",
            "label": "restrictive dermopathy 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070369",
        "DOID:0060762",
        "DOID:0070370"
    ],
    "unlinked_id_list": []
}
