About   Help   FAQ
Disease Ontology Browser
platelet-type bleeding disorder 17 (DOID:0111049)
Alliance: disease page
Synonyms: BDPLT17; hereditary thrombasthenia-thrombocytopenia
Alt IDs: OMIM:187900, ICD10CM:D69.1, MESH:D055652, NCI:C84741, UMLS_CUI:C0272302
Definition: A blood platelet disease characterized by autosomal dominant inheritance of increased bleeding tendency, gray platelets, thrombocytopenia, thrombasthenia, abnormal megakaryocytes, decreased or absent alpha-granules in platelets, and myelofibrosis that has_material_basis_in heterozygous mutation in the GFI1B gene on chromosome 9q34.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory