loading...| Preferred Name |
Scleroderma |
| ID |
http://www.orpha.net/ORDO/Orphanet_801 |
| definition |
Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc) (see these terms). |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=801 |
| has_age_of_onset |
All ages |
| has_inheritance |
Not applicable |
| hasDbXref |
MedDRA:10039710 UMLS:C0852007 |
| label |
Scleroderma |
| notation |
ORPHA:801 Clinical group |
| prefixIRI |
ORDO:Orphanet_801 |
| prefLabel |
Scleroderma |
| present_in |
Worldwide AND has_point_prevalence_average_value : 42.0 AND has_point_prevalence_range : 1-5 / 10 000 Australia AND has_point_prevalence_average_value : 23.0 AND has_point_prevalence_range : 1-5 / 10 000 Specific population AND has_point_prevalence_average_value : 469.0 AND has_point_prevalence_range : >1 / 1000 Australia AND has_annual_incidence_average_value : 1.5 AND has_annual_incidence_range : 1-9 / 100 000 Worldwide AND has_annual_incidence_average_value : 1.41 AND has_annual_incidence_range : 1-9 / 100 000 |
| subClassOf |