Search Ontology:
Human Disease

hypotrichosis 8

Term ID
DOID:0110705
Synonyms
  • hypotrichosis, localized, autosomal recessive 3
  • HYPT8
  • LAH3
Definition
A hypotrichosis has_material_basis_in a autosomal recessive mutation of the LPAR6 gene on chromosome 13q14.2. https://www.ncbi.nlm.nih.gov/pubmed/18297072
References
Ontology
Human Disease   ( DOID:0110705 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models