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loading...| Preferred Name |
Monilethrix |
| ID |
http://www.orpha.net/ORDO/Orphanet_573 |
| alternative_term |
Moniliform hair syndrome |
| definition |
A rare genodermatosis characterized by a hair shaft dysplasia resulting in hypotrichosis. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=573 |
| has_age_of_onset |
Neonatal Infancy |
| has_inheritance |
Autosomal recessive Autosomal dominant |
| hasDbXref |
ICD-10:Q84.1 OMIM:158000 ICD-11:EC21.0 UMLS:C0546966 MeSH:D056734 |
| label |
Monilethrix |
| notation |
ORPHA:573 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_573 |
| prefLabel |
Monilethrix |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
| treeView | |
| subClassOf |
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