{
    "disease_id": "DOID:0050631", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "T3 resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "X-linked intellectual disability with hypotonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "MCT8 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "Allan-Herndon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "monocarboxylate transporter-8 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "MCT8-specific Thyroid hormone cell Membrane transporter deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "monocarboxylate transporter 8 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "mental retardation, X-linked, with hypotonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "X-linked intellectual disability-hypotonia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "triiodothyronine resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "T3 resisitence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "intellectual disability and muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "AHDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "triiodothyronine resistence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "mental retardation and muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010354", 
            "name": "ALLAN-Herndon-DUDLEY syndrome; AHDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050631", 
            "name": "AHDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050631", 
            "name": "ALLAN-HERNDON SYNDROME"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050631", 
        "description": "A syndrome that has_material_basis_in mutation at is in the gene encoding the monocarboxylate transporter-8 which alters the structure and function of the SLC16A2 protein which is then unable to transport the thyroid triiodothyronine (T3) hormone into nerve cells of the developing brain affecting normal brain development resulting in intellectual disability and problems with movement.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050631", 
        "name": "Allan-Herndon-Dudley syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050631#disease-associations", 
            "id": "0050631", 
            "database": "Alliance of Genome Resources"
        }
    ]
}