OBO ID: DOID:0110698
Term Name: hypotrichosis 1 Search Ontology:
Synonyms:
  • hereditary generalized hypotrichosis simplex
  • Hhs
  • 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 )
OTHER hypotrichosis 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
APCDD1 Hypotrichosis 1 605389
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None