hypotrichosis 6

Summary

DOID:0110703 - hypotrichosis 6

Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the DSG4 gene on chromosome 18q12.1.

Synonyms: Hypotrichosis, Localized, Autosomal Recessive 1, Hypt6, Lah1, Monilethrix-like hypotrichosis, autosomal recessive localized hypotrichosis,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011932 - hypotrichosis 6

MONDO:0011932 - hypotrichosis 6

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), hypotrichosis (is_a)