Huntington's disease ICD10CM:G10 KEGG:05016 MESH:D006816 ICD9CM:333.4 HD disease_ontology GARD:6677 NCI:C82342 DOID:12858 ICD9CM_2006:333.4 OMIM:143100 CSP2005:2057-3283 UMLS_CUI:C0020179 Huntington disease SNOMEDCT_US_2018_03_01:58756001 A neurodegenerative disease that has material basis in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has material basis in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities. Huntington's chorea neurodegenerative disease