{
    "disease_id": "DOID:0060720", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011218", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "ichthyosis-follicular atrophoderma-hypotrichosis syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "IHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "hypotrichosis-congenital ichthyosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011218", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "ARCI11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "IFAH syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011218", 
            "name": "autosomal recessive ichthyosis with hypotrichosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060720", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "IFAH syndrome"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "autosomal recessive ichthyosis with hypotrichosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060720", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "hypotrichosis-congenital ichthyosis syndrome"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "ichthyosis-hypotrichosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060720", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060720", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
            "name": "ichthyosis-follicular atrophoderma-hypotrichosis syndrome"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060720", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060720", 
        "description": "An autosomal recessive congenital ichthyosis characterized by ichthyosis, hypotrichosis, photophobia, corneal opacity, pingueculum, blepharitis, marked acanthosis, otrhohyperkeratosis and hyperkeratosis that has_material_basis_in homozygous mutation in the ST14 gene on chromosome 11q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060720", 
        "name": "autosomal recessive congenital ichthyosis 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060720#disease-associations", 
            "id": "0060720", 
            "database": "Alliance of Genome Resources"
        }
    ]
}