WormBase Tree Display for DO_term: DOID:12858
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DOID:12858 | Name | Huntington's disease | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | 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. | ||||
Synonym | Exact | HD | |||
Huntington disease | |||||
Huntington's chorea | |||||
Parent | Is_a | DOID:1289 | |||
DB_info | Database | OMIM | disease | 143100 | |
Disease_model_annotation (24) | |||||
Attribute_of (9) |