{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "Hartnup disorder; HND"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "neutral amino acid transport defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "neutral 1 amino acid transport defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "deficiency of tryptophan oxygenase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "Hartnup disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "aminoaciduria, Hartnup type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009324", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009324", 
            "name": "HND"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1060", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1060", 
            "name": "Neutral 1 amino acid transport defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1060", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1060", 
            "name": "deficiency of tryptophan oxygenase"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1060", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1060", 
            "name": "neutral amino acid transport defect"
        }, 
        {
            "url": "https://www.omim.org/entry/234500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:234500", 
            "name": "Hartnup disorder"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1060", 
        "description": "An amino acid metabolic disorder that is caused by abnormalities of the renal tubules and is characterized especially by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular incoordination due to the effects of the disease on the cerebellum.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1060", 
        "name": "Hartnup disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/234500", 
            "id": "234500", 
            "database": "MIM"
        }
    ]
}