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