hereditary neuropathy with liability to pressure palsies

Summary
Synonym
  • HNPP
  • current pressure-sensitive neuropathy
  • familial recurrent polyneuropathy
  • heterozygous microdeletion 17p11.2p12
  • potato-grubbing palsy
  • tomaculous neuropathy
  • tulip-bulb digger's palsy
Definition
A neuropathy characterized by autosomal dominant inheritance of peroneal muscle weakness, peripheral neuropathy, hyporeflexia, tomacula, segmental demyelination/remyelination, decreased motor nerve conduction that has_material_basis_in deletion or point mutation of the PMP22 gene on chromosome 17p12.
Super Class
autosomal dominant disease neuropathy
External Links
Disease Ontology
DOID:0060843
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 21 - 30 of 30 in total
Gene ID Gene Symbol Description Source
8898 MTMR2 myotubularin related protein 2
9517 SPTLC2 serine palmitoyltransferase long chain base subunit 2
9896 FIG4 FIG4 phosphoinositide 5-phosphatase
10558 SPTLC1 serine palmitoyltransferase long chain base subunit 1
10855 HPSE heparanase
23175 LPIN1 lipin 1
23600 AMACR alpha-methylacyl-CoA racemase
27036 SIGLEC7 sialic acid binding Ig like lectin 7
51196 PLCE1 phospholipase C epsilon 1
84649 DGAT2 diacylglycerol O-acyltransferase 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