{"orpha":294057,"name":"Rare nevus","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-294057/","orphanet_url":"https://www.orpha.net/en/disease/detail/294057","names":{"fr":{"name":"Naevus rare"},"de":{"name":"Seltener Naevus","synonyms":["Nävus, seltener"]},"es":{"name":"Nevo raro"},"it":{"name":"Nevo raro"},"nl":{"name":"Zeldzame naevus"},"pt":{"name":"Nevo raro"},"pl":{"name":"Rzadkie znamię"},"cs":{"name":"Vzácný névus"},"uk":{"name":"Рідкісний невус"},"zh":{"name":"罕见痣"},"tr":{"name":"Nadir nevüs"}},"xrefs":[{"source":"MONDO","code":"17414","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680997","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98588,"name":"OBSOLETE: Palpebral nevus","status":"inactive"}],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":79386,"name":"Rare skin tumor or hamartoma","classifications":[187,202]}],"children":[{"orpha":370039,"name":"Angora hair nevus","type":"Disease"},{"orpha":64755,"name":"Becker nevus syndrome","type":"Disease"},{"orpha":139,"name":"CHILD syndrome","type":"Disease"},{"orpha":140944,"name":"CLOVES syndrome","type":"Malformation syndrome"},{"orpha":139414,"name":"Congenital panfollicular nevus","type":"Disease"},{"orpha":201,"name":"Cowden syndrome","type":"Clinical subtype"},{"orpha":370046,"name":"Didymosis aplasticosebacea","type":"Disease"},{"orpha":35125,"name":"Epidermal nevus syndrome","type":"Disease"},{"orpha":497737,"name":"Epidermolytic nevus","type":"Disease"},{"orpha":626,"name":"Large/giant congenital melanocytic nevus","type":"Disease"},{"orpha":2612,"name":"Linear nevus sebaceus syndrome","type":"Disease"},{"orpha":2611,"name":"Linear verrucous nevus syndrome","type":"Disease"},{"orpha":497757,"name":"MME-related autosomal dominant Charcot Marie Tooth disease type 2","type":"Disease"},{"orpha":370059,"name":"NEVADA syndrome","type":"Disease"},{"orpha":2481,"name":"Neurocutaneous melanocytosis","type":"Disease"},{"orpha":64754,"name":"Nevus comedonicus syndrome","type":"Disease"},{"orpha":263432,"name":"Nevus of Ito","type":"Disease"},{"orpha":263425,"name":"Nevus of Ota","type":"Disease"},{"orpha":313936,"name":"PENS syndrome","type":"Disease"},{"orpha":2874,"name":"Phakomatosis pigmentokeratotica","type":"Malformation syndrome"},{"orpha":166286,"name":"Porokeratotic eccrine ostial and dermal duct nevus","type":"Disease"},{"orpha":744,"name":"Proteus syndrome","type":"Malformation syndrome"},{"orpha":2969,"name":"Proteus-like syndrome","type":"Clinical subtype"},{"orpha":370052,"name":"SCALP syndrome","type":"Disease"},{"orpha":137608,"name":"Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome","type":"Clinical subtype"},{"orpha":171723,"name":"White sponge nevus","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}