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GENE - TERM ANNOTATION REPORT
2 Annotations Found.
An association has been curated linking
ADAR
and
dyschromatosis symmetrica hereditaria
in Sus scrofa.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred from sequence orthology with
ADAR (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
6
RGD objects have been annotated to
dyschromatosis symmetrica hereditaria
(DOID:0060257)
0
papers in RGD have been used to annotate
ADAR
Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
Original References(s):
PMID:12916015
PMID:15102079
PMID:15146470
PMID:15347341
PMID:15489923
PMID:15659327
PMID:15955093
PMID:16199547
PMID:16536805
PMID:16817193
PMID:16917490
PMID:16935814
PMID:17225010
PMID:17569068
PMID:17576681
PMID:18705826
PMID:19017046
PMID:19060901
PMID:20069304
PMID:20186421
PMID:20300939
PMID:20301648
PMID:20430589
PMID:20439151
PMID:21182352
PMID:21211811
PMID:21924887
PMID:21933234
PMID:22336994
PMID:22974014
PMID:23001123
PMID:24033266
PMID:24262145
PMID:24950769
PMID:25243380
PMID:25326637
PMID:25456137
PMID:25468572
PMID:25604658
PMID:25640679
PMID:25741868
PMID:25982145
PMID:26372505
PMID:26629815
PMID:26802932
PMID:26892242
PMID:27937139
PMID:28139822
PMID:28492532
PMID:28502085
PMID:28561207
PMID:29185800
PMID:29221912
PMID:29536976
PMID:29603717
PMID:29691679
PMID:29775506
PMID:29896739
PMID:29915444
PMID:30564185
PMID:30692772
PMID:30755392
PMID:31423758
PMID:31772029
PMID:32593192
PMID:32801363
PMID:32996714
PMID:33289110
PMID:33307271
PMID:33723056
PMID:34343497
PMID:34702576
PMID:34988976
PMID:35551623
PMID:35859177
PMID:8627722
PMID:9536098
PMID:9889202
An association has been curated linking
ADAR
and
dyschromatosis symmetrica hereditaria
in Sus scrofa.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with
ADAR (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
6
RGD objects have been annotated to
dyschromatosis symmetrica hereditaria
(DOID:0060257)
0
papers in RGD have been used to annotate
ADAR
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