Search Ontology:
Human Disease

hypotrichosis 12

Term ID
DOID:0110709
Synonyms
  • HYPT12
Definition
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2. https://www.ncbi.nlm.nih.gov/pubmed/21412954
References
Ontology
Human Disease   ( DOID:0110709 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models