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Namespace Prefixes

PrefixIRI
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n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0070161
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050548
rdfs:label
hereditary sensory and autonomic neuropathy type 2
wdrs:describedby
n7:doid.owl
obo:id
DOID:0070161
obo:hasDbXref
MESH:D002607 SNOMEDCT_US_2021_09_01:30508001 UMLS_CUI:C0020072 GARD:3976 UMLS_CUI:C0270914 ORDO:970 MESH:D009477
obo:hasExactSynonym
HSAN2 hereditary sensory and autonomic neuropathy type II
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood.