{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "FAO deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "FALDH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "Sjogren-Larsson syndrome; SLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "Sjogren-Larsson's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "fatty alcohol:NAD+ oxidoreductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "Sjgren-Larsson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "fatty acid alcohol oxidoreductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "Sjogren Larsson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "FADH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "fatty aldehyde dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "ichthyosis, spastic neurologic disorder, and oligophrenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010031", 
            "name": "SLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14501", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14501", 
            "name": "FALDH deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14501", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14501", 
            "name": "SLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14501", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14501", 
            "name": "Sjogren Larsson syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14501", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14501", 
            "name": "Sjogren-Larsson's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14501", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14501", 
            "name": "fatty acid alcohol oxidoreductase deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/270200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:270200", 
            "name": "Sjoegren-Larsson syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14501", 
        "description": "A syndrome that is characterized by ichthyosis, mental retardation, spastic paraparesis, macular dystrophy, and leukoencephalopathy, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the aldehyde dehydrogenase 3 family member A2 (ALDH3A2) gene, which encodes fatty aldehyde dehydrogenase, on chromosome 17p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14501", 
        "name": "Sjogren-Larsson syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/270200", 
            "id": "270200", 
            "database": "MIM"
        }
    ]
}