{
    "disease_id": "DOID:2120", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2120", 
            "name": "FDH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2120", 
            "name": "Goltz-Gorlin syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2120", 
            "name": "FODH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2120", 
            "name": "Goltz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "Goltz syndrome or focal dermal hypoplasia is characterized by a polymorphic cutaneous disorder and highly variable anomalies affecting the eyes, teeth, skeleton and the central nervous, urinary, gastrointestinal and cardiovascular systems.", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "focal dermal hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "FDH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "DHOF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "focal dermal hypoplasia; FDH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "Fodh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "Goltz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "focal dermal hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "Goltz-Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010592", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010592", 
            "name": "Goltz Gorlin syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/305600", 
            "description": "Focal dermal hypoplasia", 
            "resource": "MIM", 
            "id": "MIM:305600", 
            "name": "Focal dermal hypoplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2120", 
        "description": "A syndrome characterized at birth by streaks of very thin skin (dermal hypoplasia), cutis aplasia, and telangiectases, and has_material_basis_in heterozygous mutation in the PORCN gene on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2120", 
        "name": "focal dermal hypoplasia"
    }
}