Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 27/07/2006

Symbol	MNX
Location	12q13
Name	monilethrix
Corresponding gene	KRT81 , KRT86
Main clinical features	beaded fragile hair, dystrophic alopecia, follicular keratosis and nail defect (defect of tricho-cytokeratin)
Genetic determination	autosomal dominant
Function/system disorder	dermatology
Type	disease

Gene product

Name	keratin, hair, type II basic 2 or 6