hereditary sensory and autonomic neuropathy type 1C

Summary
Synonym
  • HSAN1C
  • hereditary sensory and autonomic neuropathy type IC
Definition
A hereditary sensory and autonomic neuropathy type 1 that has_material_basis_in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.
Super Class
autosomal dominant disease hereditary sensory and autonomic neuropathy type 1
External Links
Disease Ontology
DOID:0070157
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9517 SPTLC2 serine palmitoyltransferase long chain base subunit 2
The Human Phenotype Ontology
Displaying entries 11 - 20 of 45 in total
HPO ID HPO Term
HP:0002754 Osteomyelitis
HP:0002756 Pathologic fracture
HP:0002821 Neuropathic arthropathy
HP:0002936 Distal sensory impairment
HP:0003376 Steppage gait
HP:0003693 Distal amyotrophy
HP:0006937 Impaired distal tactile sensation
HP:0007002 Motor axonal neuropathy
HP:0007021 Pain insensitivity
HP:0007078 Decreased amplitude of sensory action potentials
Displaying all 2 entries
Gene ID Gene Symbol Description
10558 SPTLC1 serine palmitoyltransferase long chain base subunit 1
9517 SPTLC2 serine palmitoyltransferase long chain base subunit 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024