{"orpha":98027,"name":"Rare disease with odontological manifestation","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-98027/","orphanet_url":"https://www.orpha.net/en/disease/detail/98027","names":{"fr":{"name":"Maladie rare avec atteinte odontologique"},"de":{"name":"Odontologische Manifestation, seltener Krankheit mit"},"es":{"name":"Enfermedad rara con manifestación odontológica"},"it":{"name":"Malattia rara con manifestazione odontologica"},"nl":{"name":"Zeldzame ziekte met odontologische manifestatie"},"pt":{"name":"Doença rara com manifestações odontológicas"},"pl":{"name":"Rzadkie choroby z objawami stomatologicznymi"},"cs":{"name":"Vzácná onemocnění s odontologickou manifestací"},"uk":{"name":"Рідкісне захворювання з одонтологічним проявом"},"zh":{"name":"伴口腔累及的罕见疾病"},"tr":{"name":"Odontolojik belirtili nadir hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681548","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98026,"name":"Rare odontologic disease"},"parents":[{"orpha":98026,"name":"Rare odontologic disease","classifications":[197]}],"children":[{"orpha":247676,"name":"Adult hypophosphatasia","type":"Clinical subtype"},{"orpha":65282,"name":"Carvajal syndrome","type":"Disease"},{"orpha":184,"name":"Cherubism","type":"Malformation syndrome"},{"orpha":247667,"name":"Childhood-onset hypophosphatasia","type":"Clinical subtype"},{"orpha":99792,"name":"Dentin dysplasia-sclerotic bones syndrome","type":"Disease"},{"orpha":708036,"name":"Ectodermal dysplasia with agenesis of maxillary lateral incisors and mandibular anterior teeth","type":"Malformation syndrome"},{"orpha":708043,"name":"Ectodermal dysplasia with oligodontia-hand and foot malformation-hypoplastic nipples","type":"Malformation syndrome"},{"orpha":2325,"name":"Epidermolysis bullosa simplex with anodontia/hypodontia","type":"Malformation syndrome"},{"orpha":476096,"name":"Erythrokeratodermia-cardiomyopathy syndrome","type":"Disease"},{"orpha":714399,"name":"Global developmental delay-dental enamel defects-ataxia syndrome","type":"Disease"},{"orpha":377,"name":"Gorlin syndrome","type":"Malformation syndrome"},{"orpha":685067,"name":"Hypodontia-scalp hypotrichosis-facial dysmorphism syndrome","type":"Disease"},{"orpha":363523,"name":"Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome","type":"Disease"},{"orpha":238468,"name":"Hypohidrotic ectodermal dysplasia","type":"Disease"},{"orpha":98813,"name":"Hypohidrotic ectodermal dysplasia with immunodeficiency","type":"Disease"},{"orpha":464,"name":"Incontinentia pigmenti","type":"Malformation syndrome"},{"orpha":247651,"name":"Infantile hypophosphatasia","type":"Clinical subtype"},{"orpha":79402,"name":"Intermediate generalized junctional epidermolysis bullosa","type":"Disease"},{"orpha":79405,"name":"Junctional epidermolysis bullosa inversa","type":"Disease"},{"orpha":79403,"name":"Junctional epidermolysis bullosa with pyloric atresia","type":"Disease"},{"orpha":2407,"name":"Laryngo-onycho-cutaneous syndrome","type":"Disease"},{"orpha":79406,"name":"Late-onset junctional epidermolysis bullosa","type":"Disease"},{"orpha":231556,"name":"Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome","type":"Disease"},{"orpha":251393,"name":"Localized junctional epidermolysis bullosa","type":"Disease"},{"orpha":557003,"name":"Oculoskeletodental syndrome","type":"Disease"},{"orpha":247685,"name":"Odontohypophosphatasia","type":"Clinical subtype"},{"orpha":75392,"name":"Periodontal Ehlers-Danlos syndrome","type":"Disease"},{"orpha":447961,"name":"Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome","type":"Disease"},{"orpha":167762,"name":"Rare disease with dentinogenesis imperfecta","type":"Category"},{"orpha":79404,"name":"Severe generalized junctional epidermolysis bullosa","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}