OBO ID: DOID:0110706
Term Name: hypotrichosis 9 Search Ontology:
Synonyms:
  • Hypt9
Definition: A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 10q11.23-q22.3. https://www.ncbi.nlm.nih.gov/pubmed/20054564
References:
Ontology: Human Disease   ( DOID:0110706 )
Relationships
is a type of:
OTHER hypotrichosis 9 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.