Search Ontology:
Human Disease

hypotrichosis 13

Term ID
DOID:0110710
Synonyms
  • hypotrichosis with woolly hair
  • HYPT13
Definition
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the KRT71 gene on chromosome 12q13.13. https://www.ncbi.nlm.nih.gov/pubmed/22592156
References
Ontology
Human Disease   ( DOID:0110710 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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