|OBO ID: DOID:0111092|
|Term Name:||Fanconi anemia complementation group P||Search Ontology:|
|Definition:||A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3. (2)|
|Ontology:||Human Disease (DOID:0111092)|
|is a type of:||
OTHER Fanconi anemia complementation group P PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
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.