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DOID:0110699 - hypotrichosis 2
Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of CDSN on chromosome 6p21.33.
Synonyms: Htss1, Hypt2, Spanish type hypotrichosis, hypotrichosis simplex of the scalp 1,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypotrichosis (is_a)