{
    "disease_id": "DOID:0060764", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect with mesomelia, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect with mesomelia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive; RRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Covesdem syndrome, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Covesdem syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "RRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect-mesomelia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060764", 
            "name": "COVESDEM syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060764", 
            "name": "RRS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060764", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060764", 
            "name": "costovertebral segmentation defect-mesomelia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060764", 
        "description": "A Robinow syndrome characterized by autosomal recessive inheritance of severe skeletal dysplasia characterized by dysmorphic facial features, including frontal bossing, hypertelorism, and broad nose, short-limbed dwarfism, vertebral segmentation, and genital hypoplasia that has_material_basis_in homozygous or compound heterozygous mutations in the ROR2 gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060764", 
        "name": "autosomal recessive Robinow syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060764#disease-associations", 
            "id": "0060764", 
            "database": "Alliance of Genome Resources"
        }
    ]
}