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(Q66084923)
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chromosome 3-linked frontotemporal dementia
A frontotemporal dementia that has material basis in heterozygous mutation in CHMP2B on 3p11.2.
FTD3
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Statements
instance of
class of disease
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subclass of
frontotemporal dementia
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111227
genetic association
CHMP2B
0 references
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0111227
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111227
http://identifiers.org/doid/DOID:0111227
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0111227
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111227
OMIM ID
600795
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0111227
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