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General Information
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| Term |
Charcot-Marie-Tooth disease type 6 |
ID (Ontology) |
DOID:0080068 (Human Disease) |
| Definition |
A Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity. |
| Also Known As |
"hereditary motor and sensory neuropathy type 6" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 5 | | Human Disease Models (FBhh) | DOID | 2 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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Charcot-Marie-Tooth disease type 6 | 5 | 5 | 2 | ameliorates | Charcot-Marie-Tooth disease type 6 | 2 | -- | -- | for disease ribbon | Charcot-Marie-Tooth disease type 6 | -- | 4 | -- | model of | Charcot-Marie-Tooth disease type 6 | 3 | 4 | -- |
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Relationships