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.

KAZA1

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

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

Label: KAZA1

Synonyms: KAZA1, KAZA, Kala-azar (visceral leishmaniasis), susceptibility to

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

KAZA1

http://www.ncbi.nlm.nih.gov/gene/387582
MIR3074

http://www.ncbi.nlm.nih.gov/gene/100422842
C1orf167

http://www.ncbi.nlm.nih.gov/gene/284498
porokeratosis

DOID:3805
ZSWIM9

http://www.ncbi.nlm.nih.gov/gene/374920
MIR1180

http://www.ncbi.nlm.nih.gov/gene/100302256
FBXO47

http://www.ncbi.nlm.nih.gov/gene/494188
otosclerosis

DOID:12185
LOC101929705

http://www.ncbi.nlm.nih.gov/gene/101929705
X-linked endothelial corneal dystrophy

DOID:0060446
NBLST4

http://www.ncbi.nlm.nih.gov/gene/100306937
CHDS2

http://www.ncbi.nlm.nih.gov/gene/387584
LINC00687

http://www.ncbi.nlm.nih.gov/gene/728450
LINC01184

http://www.ncbi.nlm.nih.gov/gene/644873
cone dystrophy

DOID:0050795
chondrocalcinosis

DOID:1156
Scheie syndrome

DOID:0060222
DYT17

http://www.ncbi.nlm.nih.gov/gene/100216344
hereditary hypophosphatemic rickets with hypercalciuria

DOID:0050947
C6orf223

http://www.ncbi.nlm.nih.gov/gene/221416
ANP32D

http://www.ncbi.nlm.nih.gov/gene/23519
AD6

http://www.ncbi.nlm.nih.gov/gene/64851
CHCHD2P9

http://www.ncbi.nlm.nih.gov/gene/645345
no_name

http://www.ncbi.nlm.nih.gov/gene/100130503
CTD-2194D22.4

http://www.ncbi.nlm.nih.gov/gene/101929081
GAPLINC

http://www.ncbi.nlm.nih.gov/gene/100505592
mucopolysaccharidosis

DOID:12798
synpolydactyly

DOID:0060242
posterior amorphous corneal dystrophy

DOID:0060452
AGSPX

http://www.ncbi.nlm.nih.gov/gene/100188767
Schnyder corneal dystrophy

DOID:0060456
hyperpigmentation of eyelid

DOID:10122
PTCSC3

http://www.ncbi.nlm.nih.gov/gene/100886964
SELENOK

http://www.ncbi.nlm.nih.gov/gene/58515
HMGN2P46

http://www.ncbi.nlm.nih.gov/gene/283651
SNAP47

http://www.ncbi.nlm.nih.gov/gene/116841
RCD1

http://www.ncbi.nlm.nih.gov/gene/5953
angioma serpiginosum

DOID:4028
Cornelia de Lange syndrome

DOID:11725
SNORD15A

http://www.ncbi.nlm.nih.gov/gene/6079
rickets

DOID:10609
stromal dystrophy

DOID:0060442
NIDDM4

http://www.ncbi.nlm.nih.gov/gene/100188782
PSORS11

http://www.ncbi.nlm.nih.gov/gene/100271719
ZMYND8

http://www.ncbi.nlm.nih.gov/gene/23613
LOC100129940

http://www.ncbi.nlm.nih.gov/gene/100129940
Reis-Bucklers corneal dystrophy

DOID:0060453
short chain acyl-CoA dehydrogenase deficiency

DOID:0080154
AGAP7P

http://www.ncbi.nlm.nih.gov/gene/653268
subepithelial mucinous corneal dystrophy

DOID:0060454
corneal dystrophy

DOID:2566
LINC00475

http://www.ncbi.nlm.nih.gov/gene/158314
WBS2

http://www.ncbi.nlm.nih.gov/gene/7457
GGA1

http://www.ncbi.nlm.nih.gov/gene/26088
USP17L25

http://www.ncbi.nlm.nih.gov/gene/728373
juvenile rheumatoid arthritis

DOID:676
FLG-AS1

http://www.ncbi.nlm.nih.gov/gene/339400
primary cutaneous amyloidosis

DOID:0050639
MLST8

http://www.ncbi.nlm.nih.gov/gene/64223
LUNAR1

http://www.ncbi.nlm.nih.gov/gene/104564224
CTBP1-AS

http://www.ncbi.nlm.nih.gov/gene/285463
DYT13

http://www.ncbi.nlm.nih.gov/gene/93983
SM1

http://www.ncbi.nlm.nih.gov/gene/7911
PDA1

http://www.ncbi.nlm.nih.gov/gene/100996949
SNORD109A

http://www.ncbi.nlm.nih.gov/gene/338428
sclerocornea

DOID:0060252
medium chain acyl-CoA dehydrogenase deficiency

DOID:0080153
NBLST6

http://www.ncbi.nlm.nih.gov/gene/100306939
GRDX

http://www.ncbi.nlm.nih.gov/gene/117189
DMTN

http://www.ncbi.nlm.nih.gov/gene/2039
C15orf38-AP3S2

http://www.ncbi.nlm.nih.gov/gene/100526783
FECD7

http://www.ncbi.nlm.nih.gov/gene/100380875
ASPG1

http://www.ncbi.nlm.nih.gov/gene/431710
cerebral amyloid angiopathy

DOID:9246
OMS

http://www.ncbi.nlm.nih.gov/gene/619538
BAGE4

http://www.ncbi.nlm.nih.gov/gene/85317
SNORD3A

http://www.ncbi.nlm.nih.gov/gene/780851
AFG3L1P

http://www.ncbi.nlm.nih.gov/gene/172
CHEBI:549708

http://aber-owl.net/drug/CID111249762
C21orf91

http://www.ncbi.nlm.nih.gov/gene/54149
Thiel-Behnke corneal dystrophy

DOID:0060455
NBLST5

http://www.ncbi.nlm.nih.gov/gene/100306938
orbital tenonitis

DOID:11233
HYT3

http://www.ncbi.nlm.nih.gov/gene/387575
TBC1D3C

http://www.ncbi.nlm.nih.gov/gene/414060
AATBC

http://www.ncbi.nlm.nih.gov/gene/284837
HBFQTL4

http://www.ncbi.nlm.nih.gov/gene/171515
MIR1275

http://www.ncbi.nlm.nih.gov/gene/100302123
no_name

DOID:13304
PRYP3

http://www.ncbi.nlm.nih.gov/gene/442865
HSD11B1L

http://www.ncbi.nlm.nih.gov/gene/374875
ANKRD36

http://www.ncbi.nlm.nih.gov/gene/375248
WHCR

http://www.ncbi.nlm.nih.gov/gene/7467
IGHV1-68

http://www.ncbi.nlm.nih.gov/gene/28462
nemaline myopathy

DOID:3191
congenital myopathy

DOID:0080100
PRINS

http://www.ncbi.nlm.nih.gov/gene/100169750
FAM47E

http://www.ncbi.nlm.nih.gov/gene/100129583
idiopathic scoliosis

DOID:0060250
LOC101928236

http://www.ncbi.nlm.nih.gov/gene/101928236

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