|  Help  |  About  |  Contact Us

DO Term : hypotrichosis 14 [DOID:0080582] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hypotrichosis that is characterized by sparse to absent lanugo-like scalp hair, sparse and brittle eyebrows, and sparse eyelashes and body hair and that has_material_basis_in homozygous or compound heterozygous mutation in the LSS gene on chromosome 21q22.
  • synonyms:
  • OMIM:618275,
  • 618275
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents