{
    "disease_id": "DOID:0111373", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "hyperpigmentation with or without hypopigmentation, familial progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "melanosis universalis hereditaria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "hyperpigmentation with or without hypopigmentation, familial progressive; FPHH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "hyperpigmentation, familial progressive, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "FPHH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "macules, hereditary congenital hypopigmented and hyperpigmented"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "melanosis, universal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007771", 
            "name": "hyperpigmentation, familial progressive, 2, formerly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111373", 
            "name": "FPHH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111373", 
            "name": "MUH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111373", 
            "name": "melanosis universalis hereditaria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111373", 
        "description": "A skin disease characterized by progressive, diffuse hyperpigmentation of variable intensity sometimes associated with cafe-au-lait macules and larger hypopigmented ash-leaf macules that has_material_basis_in heterozygous mutation in KITLG on chromosome 12q21.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111373", 
        "name": "familial progressive hyperpigmentation with or without hypopigmentation"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111373#disease-associations", 
            "id": "0111373", 
            "database": "Alliance of Genome Resources"
        }
    ]
}