Search Ontology:
Human Disease

hypotrichosis 7

Term ID
DOID:0110704
Synonyms
  • hypotrichosis, localized, autosomal recessive 2
  • HYPT7
  • LAH2
  • total hyptrichosis, Mari type
Definition
A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the LIPH gene on chromosome 3q27.2. https://www.ncbi.nlm.nih.gov/pubmed/20393562
References
Ontology
Human Disease   ( DOID:0110704 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models