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
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
20773 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:0002020 Gastroesophageal reflux
HP:0012735 Cough
HP:0002540 Inability to walk
HP:0007002 Motor axonal neuropathy
HP:0000365 Hearing impairment
HP:0002821 Neuropathic arthropathy
HP:0007550 Hypohidrosis or hyperhidrosis
HP:0001324 Muscle weakness
HP:0010834 Trophic changes related to pain
HP:0002460 Distal muscle weakness
Displaying all 3 entries
Gene ID Gene Symbol Description
10558 SPTLC1 serine palmitoyltransferase long chain base subunit 1
25923 ATL3 atlastin GTPase 3
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: December 9, 2024