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DOID:0110029 - alpha thalassemia-intellectual disability syndrome type 1
Disease Ontology 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.
Synonyms: ATR syndrome linked to chromosome 16, ATR syndrome, deletion type, ATR-16 syndrome, 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,
Echinobase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
alpha thalassemia (is_a)