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General Information
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| Term |
Charcot-Marie-Tooth disease type 2DD |
ID (Ontology) |
DOID:0111558 (Human Disease) |
| Definition |
A Charcot-Marie-Tooth disease type 2 characterized by neuropathy mainly affecting the lower limbs that has_material_basis_in heterozygous mutation in the ATP1A1 gene on chromosome 1p13.1. |
| Also Known As |
"ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2" ; "ATP1A1-related CMT2" ; "Charcot-Marie-Tooth disease, axonal, type 2DD" (for all, see Synonyms field below) |
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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 | 6 | | Human Disease Models (FBhh) | DOID | 1 |
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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 2DD | 6 | 2 | 1 | for disease ribbon | Charcot-Marie-Tooth disease type 2DD | -- | 2 | -- | model of | Charcot-Marie-Tooth disease type 2DD | 6 | 2 | -- |
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Relationships