Preferred Name |
Autonomic Neuropathy |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27033 |
code |
C27033 |
DEFINITION |
An inherited or acquired peripheral neuropathy affecting the autonomic nervous system. It results in disruption of the involuntary body functions. Inherited causes include Fabry disease and porphyrias. Acquired causes include diabetes, uremia, hepatic disorders, vitamin deficiencies, toxins, and drug toxicities. |
label |
Autonomic Neuropathy |
Legacy_Concept_Name |
Autonomic_Neuropathy |
Preferred_Name |
Autonomic Neuropathy |
prefixIRI |
C27033 |
prefLabel |
Autonomic Neuropathy |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0259749 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/OMIM/MTHU052930 | Online Mendelian Inheritance in Man | LOOM | |
http://purl.obolibrary.org/obo/DOID_11504 | Human Disease Ontology 123 | LOOM |