{
    "disease_id": "DOID:0111373",
    "recommended_name": {
        "id": "DOID:0111373",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111373",
        "name": "familial progressive hyperpigmentation with or without hypopigmentation",
        "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 the KITLG gene on chromosome 12q21.32."
    },
    "synonyms": [
        {
            "id": "DOID:0111373",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111373",
            "name": "FPHH",
            "description": ""
        },
        {
            "id": "DOID:0111373",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111373",
            "name": "MUH",
            "description": ""
        },
        {
            "id": "DOID:0111373",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111373",
            "name": "melanosis universalis hereditaria",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "hyperpigmentation with or without hypopigmentation, familial progressive",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "hyperpigmentation with or without hypopigmentation",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "hyperpigmentation with or without hypopigmentation, familial progressive",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "macules, hereditary congenital hypopigmented and hyperpigmented",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "melanosis, universal",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "FPHH",
            "description": ""
        },
        {
            "id": "MONDO:0007771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007771",
            "name": "hyperpigmentation, familial progressive, 2",
            "description": ""
        },
        {
            "id": "MIM:145250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/145250",
            "name": "Hyperpigmentation with or without hypopigmentation, familial progressive",
            "description": "Hyperpigmentation with or without hypopigmentation, familial progressive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111373"
    ],
    "unlinked_id_list": []
}