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(Q66084878)
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English
familial hemiplegic migraine 3
A familial hemiplegic migraine that has material basis in heterozygous mutation in SCN1A on 2q24.3.
MHP3
FHM3
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Statements
instance of
class of disease
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subclass of
familial hemiplegic migraine
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111183
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0111183
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111183
http://identifiers.org/doid/DOID:0111183
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0111183
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111183
GARD rare disease ID
10974
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0111183
Mondo ID
MONDO_0012320
0 references
OMIM ID
609634
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0111183
UniProt disease ID
DI-01572
0 references
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