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General Information
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| Term |
hereditary sensory and autonomic neuropathy type 1A |
ID (Ontology) |
DOID:0070152 (Human Disease) |
| Definition |
A hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has_material_basis_in heterozygous mutation in the SPTLC1 gene on chromosome 9q22. |
| Also Known As |
"hereditary sensory and autonomic neuropathy type IA" ; "HSAN1A" |
| 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 | 3 | | 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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hereditary sensory and autonomic neuropathy type 1A | 3 | 1 | 1 | for disease ribbon | hereditary sensory and autonomic neuropathy type 1A | -- | 1 | -- | model of | hereditary sensory and autonomic neuropathy type 1A | 3 | 1 | -- |
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Relationships