Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3338681> ?p ?o }
- Q3338681 subject Q13276590.
- Q3338681 subject Q6853484.
- Q3338681 subject Q7215448.
- Q3338681 abstract "Hereditary sensory and autonomic neuropathy type I (HSAN I) or hereditary sensory neuropathy type I (HSN I) is a group of autosomal dominant inherited neurological diseases that affect the peripheral nervous system particularly on the sensory and autonomic functions. The hallmark of the disease is the marked loss of pain and temperature sensation in the distal parts of the lower limbs. The autonomic disturbances, if present, manifest as sweating abnormalities.The beginning of the disease varies between adolescence and adulthood. Since affected individuals cannot feel pain, minor wounds or blisters in the painless area may not be immediately recognized and can develop into extensive and deep foot ulcerations. Once infection occurs, the complications such as inflammation and progressive destruction of the underlying bones may follow and may require amputation of the surrounding area.HSAN I is the most common type among the five types of HSAN. As a heterogeneous group of diseases, HSAN I can be divided into five subtypes HSAN IA-E. Most of the genes associated with the diseases have been identified. However, the molecular pathways leading to the manifestation of the diseases are not fully understood. Therefore, the potential targets for therapeutic interventions are not known. Moreover, gene-based therapies for patients with the diseases are not available to date, hence supportive care is the only treatment available for the patients.".
- Q3338681 icd10 "G60.8".
- Q3338681 icd9 "356.8".
- Q3338681 omim "162400".
- Q3338681 wikiPageExternalLink hereditary-sensory-and-autonomic-neuropathy-type-v.
- Q3338681 wikiPageExternalLink mostgene.org.
- Q3338681 wikiPageExternalLink GARD.
- Q3338681 wikiPageExternalLink diseases.
- Q3338681 wikiPageExternalLink degeneration.
- Q3338681 wikiPageExternalLink Default.cfm.
- Q3338681 wikiPageExternalLink NBK1180.
- Q3338681 wikiPageExternalLink NBK1390.
- Q3338681 wikiPageExternalLink NBK1769.
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