Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

WBS2

ID: http://www.ncbi.nlm.nih.gov/gene/7457

Type: http://bio2vec.net/ontology/gene

Label: WBS2

Synonyms: WBS2, WBS, WS, Williams-Beuren syndrome type 2

Alternative IDs: 7457

API: GO

SPARQL: GO

Similar Entities

WBS2

http://www.ncbi.nlm.nih.gov/gene/7457
TRIM74

http://www.ncbi.nlm.nih.gov/gene/378108
DUP7Q11.23

http://www.ncbi.nlm.nih.gov/gene/100240730
TRIM50

http://www.ncbi.nlm.nih.gov/gene/135892
TRIM73

http://www.ncbi.nlm.nih.gov/gene/375593
IGHV3-33

http://www.ncbi.nlm.nih.gov/gene/28434
red-green color blindness

DOID:13909
DYT2

http://www.ncbi.nlm.nih.gov/gene/1862
cranial nerve disease

DOID:5656
Williams-Beuren syndrome

DOID:1928
MAGEA12

http://www.ncbi.nlm.nih.gov/gene/4111
crater-like holes of optic disc

DOID:13295
trochlear nerve disease

DOID:13864
DBIL5P2

http://www.ncbi.nlm.nih.gov/gene/100169989
prosopagnosia

DOID:4970
Herpes simplex virus esophagitis

DOID:6296
staphyloma posticum

DOID:13789
Riley-Day syndrome

DOID:11589
ametropic amblyopia

DOID:10377
LOC101928791

http://www.ncbi.nlm.nih.gov/gene/101928791
SNORD3A

http://www.ncbi.nlm.nih.gov/gene/780851
peripheral retinal degeneration

DOID:12161
NR1I4

http://www.ncbi.nlm.nih.gov/gene/22817
renal glycosuria

DOID:9432
MAGEB1

http://www.ncbi.nlm.nih.gov/gene/4112
olfactory nerve disease

DOID:367
Borjeson-Forssman-Lehmann syndrome

DOID:0050681
myotonic cataract

DOID:82
BCC3

http://www.ncbi.nlm.nih.gov/gene/100307120
Herpes simplex virus keratitis

DOID:9195
glossopharyngeal nerve disease

DOID:3418
no_name

DOID:291
C20orf194

http://www.ncbi.nlm.nih.gov/gene/25943
HYT3

http://www.ncbi.nlm.nih.gov/gene/387575
third cranial nerve disease

DOID:562
GTF2IRD2

http://www.ncbi.nlm.nih.gov/gene/84163
sagittal sinus thrombosis

DOID:3576
All

HP:0000001
LOC102724159

http://www.ncbi.nlm.nih.gov/gene/102724159
secondary Parkinson disease

DOID:13548
chromosome 15q25 deletion syndrome

DOID:0060396
exophthalmos

DOID:9370
diabetic encephalopathy

DOID:0050850
MIR1260A

http://www.ncbi.nlm.nih.gov/gene/100302236
no_name

DOID:10750
no_name

DOID:12767
herpes zoster

DOID:8536
blue color blindness

DOID:11661
active vestibular Meniere'\''s disease

DOID:13491
mucopolysaccharidosis

DOID:12798
Cri-Du-Chat syndrome

DOID:12580
supravalvular aortic stenosis

DOID:1929
Blessig'\''s cysts

DOID:12164
Wernicke-Korsakoff syndrome

DOID:10915
HLA-DRB2

http://www.ncbi.nlm.nih.gov/gene/3124
hypertensive encephalopathy

DOID:9427
DNAJA1P5

http://www.ncbi.nlm.nih.gov/gene/94236
no_name

DOID:9817
ocular motility disease

DOID:1279
no_name

DOID:3802
keratoconjunctivitis sicca

DOID:12895
fundus dystrophy

DOID:8501
IGHV3-76

http://www.ncbi.nlm.nih.gov/gene/28406
Wolf-Hirschhorn syndrome

DOID:0050460
no_name

DOID:9367
achromatopsia

DOID:13911
LOC101927437

http://www.ncbi.nlm.nih.gov/gene/101927437
KAZA1

http://www.ncbi.nlm.nih.gov/gene/387582
no_name

http://www.ncbi.nlm.nih.gov/gene/100500805
oromandibular dystonia

DOID:0050843
DAD1P1

http://www.ncbi.nlm.nih.gov/gene/56286
no_name

DOID:9106
inhibited male orgasm

DOID:5576
anterior ischemic optic neuropathy

DOID:12010
CHEBI:413057

http://aber-owl.net/drug/CID111347517
ERVK-8

http://www.ncbi.nlm.nih.gov/gene/619465
scotoma

DOID:9335
visual pathway disease

DOID:1393
pupil disease

DOID:238
chromosomal deletion syndrome

DOID:0060388
NANOGP1

http://www.ncbi.nlm.nih.gov/gene/404635
Leber hereditary optic neuropathy

DOID:705
postencephalitic Parkinson disease

DOID:14332
SNORD109B

http://www.ncbi.nlm.nih.gov/gene/338429
Immucillin-G

http://aber-owl.net/drug/CID100001334
cystinosis

DOID:1064
uterine cervix leukoplakia

DOID:9043
oculomotor nerve paralysis

DOID:11550
WHAMMP3

http://www.ncbi.nlm.nih.gov/gene/339005
LINC02580

http://www.ncbi.nlm.nih.gov/gene/100506047
vasculogenic impotence

DOID:4762
cobblestone retinal degeneration

DOID:12166
hypotropia

DOID:9841
presbyopia

DOID:11638
pharyngoconjunctival fever

DOID:13801
PRBNS

http://www.ncbi.nlm.nih.gov/gene/100301572
C4orf48

http://www.ncbi.nlm.nih.gov/gene/401115
BMND7

http://www.ncbi.nlm.nih.gov/gene/100188853
RLS6

http://www.ncbi.nlm.nih.gov/gene/100302512
FLJ16779

http://www.ncbi.nlm.nih.gov/gene/100192386

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