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loading...| Preferred Name |
Alopecia universalis |
| ID |
http://www.orpha.net/ORDO/Orphanet_701 |
| definition |
A disorder of most severe form of alopecia areata, an inflammatory disease of the hair follicle, which is characterized by a complete loss of hair of the scalp and all the hair-bearing areas of the body. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=701 |
| has_age_of_onset |
All ages |
| has_inheritance |
Autosomal recessive Multigenic/multifactorial |
| hasDbXref |
MedDRA:10001767 OMIM:104000 UMLS:C0263505 ICD-10:L63.1 ICD-11:ED70.2Y MeSH:C537055 OMIM:203655 OMIM:610753 |
| label |
Alopecia universalis |
| notation |
ORPHA:701 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_701 |
| prefLabel |
Alopecia universalis |
| present_in |
Europe AND has_point_prevalence_average_value : 25.0 AND has_point_prevalence_range : 1-5 / 10 000 |
| treeView | |
| subClassOf |
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