About   Help   FAQ
Disease Ontology Browser
hereditary spherocytosis type 1 (DOID:0110916)
Alliance: disease page
Synonyms: hereditary spherocytosis 1; HS1; SPH1
Alt IDs: OMIM:182900
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the ANK1 gene on chromosome 8p11.21.

Disease References using Mouse Models (11)
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
11/12/2024
MGI 6.24 		The Jackson Laboratory