{
    "disease_id": "DOID:0080751",
    "recommended_name": {
        "id": "DOID:0080751",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080751",
        "name": "keratosis pilaris atrophicans",
        "description": "An ichthyosis that is characterized by perifollicular keratosis and inflammation that progresses to atrophy and scarring of the facial skin."
    },
    "synonyms": [
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "keratosis pilaris atrophicans",
            "description": "An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair."
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "keratosis pilaris atrophicans",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "Atrophodermia reticulata",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "Atrophodermia reticulata symmetrica faciei",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "Atrophodermia vermiculata",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "KPA",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "burnett Schwartz Berberian syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "folliculitis ulerythematosa",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "folliculitis ulerythematosa reticulata",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "honeycomb atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "keratosis pilaris",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "keratosis pilaris atrophicans facies",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "ulerythema ophryogenes",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "ulerythema ophryogenes with multiple congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0018855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018855",
            "name": "ulerythema ophryogenesis",
            "description": ""
        },
        {
            "id": "MIM:604093",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604093",
            "name": "Keratosis pilaris atrophicans",
            "description": "Keratosis pilaris atrophicans"
        }
    ],
    "children": [
        {
            "id": "DOID:0080753",
            "label": "keratosis follicularis spinulosa decalvans",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0080754",
                    "label": "X-linked keratosis follicularis spinulosa decalvans",
                    "link_status": true,
                    "children": []
                }
            ]
        }
    ],
    "id_list": [
        "DOID:0080754",
        "DOID:0080753",
        "DOID:0080751"
    ],
    "unlinked_id_list": []
}