Search Ontology:
Human Disease

hypotrichosis 1

Term ID
DOID:0110698
Synonyms
  • hereditary generalized hypotrichosis simplex
  • HTS
  • HYPT1
Definition
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the APCDD1 gene on chromosome 18p11.22. https://www.ncbi.nlm.nih.gov/pubmed/10878665
References
Ontology
Human Disease   ( DOID:0110698 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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