| General Information | |||
|---|---|---|---|
| Term | hereditary sensory and autonomic neuropathy type 2 | ID (Ontology) | DOID:0070161 (Human Disease) |
| Definition | A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood. | ||
| Also Known As | "hereditary sensory and autonomic neuropathy type II" ; "HSAN2" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| 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
|
|||
|
No relevant statements available
|
|||
|
||||||
neuropathy |__hereditary sensory neuropathy |__hereditary sensory and autonomic neuropathy type 2 3 rec. |__hereditary sensory and autonomic neuropathy type 2A 1 rec. |__hereditary sensory and autonomic neuropathy type 2B |__hereditary sensory neuropathy type 2C 2 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | hereditary sensory neuropathy | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:3976 MESH:D002607 MESH:D009477 ORDO:970 SNOMEDCT_US_2023_03_01:30508001 UMLS_CUI:C0020072 UMLS_CUI:C0270914 |
|||