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About:
hereditary spastic paraplegia 34
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An Entity of Type :
owl:Class
, within Data Space :
demo.openlinksw.com
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
X-linked recessive disease
hereditary spastic paraplegia
nodeID://b50943649
label
hereditary spastic paraplegia 34
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0110785
database_cross_reference
ICD10CM:G11.4
OMIM:300750
ORDO:171607
has_exact_synonym
SPG34
(en)
X-linked spastic paraplegia 34
(en)
X-linked spastic paraplegia type 34
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq24-q25.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50943650
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