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General Information
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| Term |
hereditary sensory and autonomic neuropathy type 2A |
ID (Ontology) |
DOID:0070155 (Human Disease) |
| Definition |
A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has_material_basis_in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13. |
| Also Known As |
"hereditary sensory and autonomic neuropathy type IIA" ; "HSAN2A" |
| 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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No relevant records available
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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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| Genes |
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hereditary sensory and autonomic neuropathy type 2A | 1 | for disease ribbon | hereditary sensory and autonomic neuropathy type 2A | 1 | model of | hereditary sensory and autonomic neuropathy type 2A | 1 |
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