{
    "disease_id": "DOID:14764", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:14764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14764", 
            "name": "dominant larsen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "Larsen syndrome (LS) is a rare skeletal dysplasia characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis, spatula-shaped distal phalanges and distinctive craniofacial abnormalities, including cleft palate.", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "Larsen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "Larsen syndrome; LRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "Larsen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "LRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "dominant Larsen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007875", 
            "name": "autosomal dominant Larsen syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/150250", 
            "description": "Larsen syndrome", 
            "resource": "MIM", 
            "id": "MIM:150250", 
            "name": "Larsen syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14764", 
        "description": "Asyndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14764", 
        "name": "Larsen syndrome"
    }
}