Preferred Name

Xeroderma pigmentosum

ID

http://www.orpha.net/ORDO/Orphanet_910

definition

Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV) (see these terms).

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=910

has_age_of_onset

All ages

has_inheritance

Autosomal recessive

hasDbXref

MeSH:D014983

OMIM:278760

MedDRA:10048220

OMIM:194400

ICD-11:LD27.1

OMIM:278700

OMIM:610651

OMIM:278730

UMLS:C0043346

OMIM:278780

OMIM:278720

ICD-10:Q82.1

OMIM:278740

label

Xeroderma pigmentosum

notation

ORPHA:910

part_of

http://www.orpha.net/ORDO/Orphanet_98641

http://www.orpha.net/ORDO/Orphanet_363245

http://www.orpha.net/ORDO/Orphanet_183490

http://www.orpha.net/ORDO/Orphanet_519270

http://www.orpha.net/ORDO/Orphanet_522530

http://www.orpha.net/ORDO/Orphanet_98097

http://www.orpha.net/ORDO/Orphanet_183422

http://www.orpha.net/ORDO/Orphanet_139027

http://www.orpha.net/ORDO/Orphanet_79390

http://www.orpha.net/ORDO/Orphanet_139033

http://www.orpha.net/ORDO/Orphanet_522548

http://www.orpha.net/ORDO/Orphanet_98571

http://www.orpha.net/ORDO/Orphanet_611314

prefixIRI

ORDO:Orphanet_910

prefLabel

Xeroderma pigmentosum

present_in

France AND has_birth_prevalence_average_value : 0.34 AND has_birth_prevalence_range : 1-9 / 1 000 000

United States AND has_point_prevalence_average_value : 0.1 AND has_point_prevalence_range : 1-9 / 1 000 000

United Kingdom AND has_birth_prevalence_average_value : 0.19 AND has_birth_prevalence_range : 1-9 / 1 000 000

Libyan Arab Jamahiriya AND has_annual_incidence_average_value : 1.75 AND has_annual_incidence_range : 1-9 / 100 000

Japan AND has_point_prevalence_average_value : 4.5 AND has_point_prevalence_range : 1-9 / 100 000

Germany AND has_birth_prevalence_average_value : 0.18 AND has_birth_prevalence_range : 1-9 / 1 000 000

Italy AND has_birth_prevalence_average_value : 0.16 AND has_birth_prevalence_range : 1-9 / 1 000 000

Europe AND has_birth_prevalence_average_value : 0.23 AND has_birth_prevalence_range : 1-9 / 1 000 000

Netherlands AND has_birth_prevalence_average_value : 0.41 AND has_birth_prevalence_range : 1-9 / 1 000 000

treeView

http://www.orpha.net/ORDO/Orphanet_98641

http://www.orpha.net/ORDO/Orphanet_363245

http://www.orpha.net/ORDO/Orphanet_183490

http://www.orpha.net/ORDO/Orphanet_519270

http://www.orpha.net/ORDO/Orphanet_522530

http://www.orpha.net/ORDO/Orphanet_98097

http://www.orpha.net/ORDO/Orphanet_183422

http://www.orpha.net/ORDO/Orphanet_139027

http://www.orpha.net/ORDO/Orphanet_79390

http://www.orpha.net/ORDO/Orphanet_139033

http://www.orpha.net/ORDO/Orphanet_522548

http://www.orpha.net/ORDO/Orphanet_98571

http://www.orpha.net/ORDO/Orphanet_611314

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD11CN/LD27.1 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/MESH/D014983 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/ICD10/Q82.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q82.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://www.orpha.net/ORDO/Orphanet_910 Experimental Factor Ontology / 实验性因素本体 SAME_URI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3452 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0019600 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0019600 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/DOID_0050427 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0050427 Human Disease Ontology / 人类疾病本体 LOOM