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| Term | hereditary ataxia | ID (Ontology) | DOID:0050951 (Human Disease) |
| Definition | A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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central nervous system disease |__neurodegenerative disease |__hereditary ataxia 1254 rec. |__autosomal dominant sensory ataxia 1 |__cerebellar ataxia 1092 rec. | |__autosomal dominant cerebellar ataxia(+) 895 rec. | |__autosomal recessive cerebellar ataxia(+) 209 rec. |__episodic ataxia 28 rec. | |__episodic ataxia type 1 3 rec. | |__episodic ataxia type 2 1 rec. | |__episodic ataxia type 3 | |__episodic ataxia type 4 | |__episodic ataxia type 5 1 rec. | |__episodic ataxia type 6 21 rec. | |__episodic ataxia type 7 | |__episodic ataxia type 8 | |__episodic ataxia type 9 1 rec. |__spastic ataxia 10 rec. | |__spastic ataxia 1 1 rec. | |__spastic ataxia 2 1 rec. | |__spastic ataxia 3 2 rec. | |__spastic ataxia 4 2 rec. | |__spastic ataxia 5 2 rec. | |__spastic ataxia 7 | |__spastic ataxia 8 1 rec. |__X-linked hereditary ataxia 130 rec. |__fragile X-associated tremor/ataxia syndrome 129 rec. |__X-linked cerebellar ataxia(+) 1 rec. |
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| Is a | neurodegenerative disease | ||
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External Crossreferences & Linkouts
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| GARD:6614 | |||