About   Help   FAQ
Disease Ontology Browser
infantile hypophosphatasia (DOID:0110914)
Alliance: disease page
Synonyms: Hops; phosphoethanolaminuria
Alt IDs: OMIM:241500, ORDO:247651
Definition: A hypophosphatasia that has_material_basis_in an autosomal recessive mutation of ALPL on chromosome 1p36.12.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory