About   Help   FAQ
Disease Ontology Browser
alpha thalassemia-intellectual disability syndrome type 1 (DOID:0110029)
Synonyms: alpha thalassemia-intellectual disability syndrome, deletion type; alpha thalassemia-retardation syndrome; alpha-thalassemia-intellectual disability syndrome linked to chromosome 16; alpha-thalassemia/mental retardation syndrome, deletion-type; alpha-thalassemia/mental retardation syndrome, type 1; ATR syndrome linked to chromosome 16; ATR syndrome, deletion type; ATR-16 syndrome
Alt IDs: OMIM:141750, ICD10CM:D56.0, ORDO:98791
Definition: An alpha thalassemia that has material basis in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others.


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
06/13/2017
MGI 6.10
The Jackson Laboratory