{
    "disease_id": "DOID:0111350", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "mirror hands and feets-nasal defects syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "laurin-Sandrow syndrome, segmental"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "mirror-Image polydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "laurin Sandrow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "LSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "laurin-Sandrow syndrome; LSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "Sandrow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "fibula ulna duplication tibia radius absence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "mirror hands and feet with nasal defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "tetramelic mirror-Image polydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007615", 
            "name": "fibula and ulna, Duplication of, with absence of tibia and radius"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "MIPduplication of fibuland ulna with absence of tibia and radius"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "Sandrow syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "TMIP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "miccor hands and feet with nasal defects"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "mirror hands and feets-nasal defects syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "mirror-image polydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111350", 
            "name": "tetramelic mirror-image polydactyly"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111350", 
        "description": "A dysostosis characterized by polysyndactyly of hands and/or feet, mirror image duplication of the feet, nasal defects, and loss of identity between fibula and tibia that has_material_basis_in heterozygous inheritance of small (less than 80kb) duplications in a SHH regulatory element located in intron 5 of LMBR1 on chromosome 7q36.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111350", 
        "name": "Laurin-Sandrow syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/135750", 
            "id": "135750", 
            "database": "MIM"
        }
    ]
}