Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3198
Gene Symbol: HOXA1
HOXA1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.390 Biomarker CTD_human Mice with null mutations of Hoxa1 or Hoxb1, two genes critical to hindbrain development, have phenotypic features frequently observed in autism, but no naturally occurring variants of either gene have been identified in mammals. 11091361

2000