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.

HSCR9

ID: http://www.ncbi.nlm.nih.gov/gene/100188850

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

Label: HSCR9

Synonyms: HSCR9, Hirschsprung disease, susceptibility to, 9

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

HSCR9

http://www.ncbi.nlm.nih.gov/gene/100188850
HSCR5

http://www.ncbi.nlm.nih.gov/gene/404720
Hirschsprung'\''s disease

DOID:10487
HSCR6

http://www.ncbi.nlm.nih.gov/gene/246321
HSCR7

http://www.ncbi.nlm.nih.gov/gene/246322
NSUN7

http://www.ncbi.nlm.nih.gov/gene/79730
no_name

DOID:1771
HSCR8

http://www.ncbi.nlm.nih.gov/gene/404719
Galloway-Mowat syndrome

DOID:0060364
Hypoventilation

HP:0002791
pulmonary alveolar proteinosis

DOID:12120
Neonatal breathing dysregulation

HP:0002790
fibular hypoplasia and complex brachydactyly

DOID:0050790
congenital secretory chloride diarrhea 1

DOID:0060296
Perrault syndrome

DOID:0050857
Breathing dysregulation

HP:0005957
Meier-Gorlin syndrome

DOID:0060306
HPE8

http://www.ncbi.nlm.nih.gov/gene/619406
Usher syndrome

DOID:0050439
CLRN1-AS1

http://www.ncbi.nlm.nih.gov/gene/116933
Nocturnal hypoventilation

HP:0002877
Warburg micro syndrome

DOID:0060237
central sleep apnea

DOID:9220
nephronophthisis

DOID:12712
juvenile rheumatoid arthritis

DOID:676
LOC647859

http://www.ncbi.nlm.nih.gov/gene/647859
UV-sensitive syndrome

DOID:0060240
MT2P1

http://www.ncbi.nlm.nih.gov/gene/4503
trochlear nerve disease

DOID:13864
megacolon

DOID:11372
tripeptide-based inhibitor

http://aber-owl.net/drug/CID109829396
Aicardi-Goutieres syndrome

DOID:0050629
cornea plana

DOID:0060287
SureCN7273831

http://aber-owl.net/drug/CID010076806
no_name

DOID:10129
urofacial syndrome

DOID:0050816
complement component 7 deficiency

DOID:0060300
Duodenal aganglionosis

HP:0011465
Aganglionosis of the small intestine

HP:0011464
Hermansky-Pudlak syndrome

DOID:3753
Hypopnea

HP:0040213
X-linked endothelial corneal dystrophy

DOID:0060446
complement component 9 deficiency

DOID:0060303
type II complement component 8 deficiency

DOID:0060302
salt and pepper syndrome

DOID:0060470
Hermansky-Pudlak syndrome 1

DOID:0060539
ENO4

http://www.ncbi.nlm.nih.gov/gene/387712
megalocornea

DOID:0060305
vesiculitis

DOID:9365
complement component 4a deficiency

DOID:0060297
Cogan-Reese syndrome

DOID:0060217
IGHV3-76

http://www.ncbi.nlm.nih.gov/gene/28406
hydrolethalus syndrome

DOID:0050779
hydrocephalus

DOID:10908
LINC00470

http://www.ncbi.nlm.nih.gov/gene/56651
gonococcal seminal vesiculitis

DOID:10400
no_name

DOID:0050076
Schnyder corneal dystrophy

DOID:0060456
cystoid macular retinal degeneration

DOID:14245
type I complement component 8 deficiency

DOID:0060301
CHARGE syndrome

DOID:0050834
CHEBI:400077

http://aber-owl.net/drug/CID044388959
subepithelial mucinous corneal dystrophy

DOID:0060454
FUSE

http://www.ncbi.nlm.nih.gov/gene/2522
Haemophilus influenzae pneumonia

DOID:10527
Central hypoventilation

HP:0007110
eye degenerative disease

DOID:9799
colorectal adenoma

DOID:0050860
Chronic lymphocytic meningitis

HP:0007041
GTF2IP1

http://www.ncbi.nlm.nih.gov/gene/2970
complement component 6 deficiency

DOID:0060299
Meesmann corneal dystrophy

DOID:0060451
breast adenoid cystic carcinoma

DOID:4877
Episodic hypoventilation

HP:0004881
AACS

http://www.ncbi.nlm.nih.gov/gene/65985
MIRLET7I

http://www.ncbi.nlm.nih.gov/gene/406891
megacystis-microcolon-intestinal hypoperistalsis syndrome

DOID:0060610
SCA18

http://www.ncbi.nlm.nih.gov/gene/94008
RNU6ATAC

http://www.ncbi.nlm.nih.gov/gene/100151684
epiphora due to excess lacrimation

DOID:14244
CHEBI:398210

http://aber-owl.net/drug/CID111232464
allergic gastroenteritis and colitis

DOID:8807
chromosome 1p36 deletion syndrome

DOID:0060410
DNPH1

http://www.ncbi.nlm.nih.gov/gene/10591
TRAV4

http://www.ncbi.nlm.nih.gov/gene/28689
posterior amorphous corneal dystrophy

DOID:0060452
retinal dystrophies primarily involving Bruch'\''s membrane

DOID:13227
3MC syndrome 3

DOID:0060577
LOC101927437

http://www.ncbi.nlm.nih.gov/gene/101927437
Vici syndrome

DOID:0060356
bovine respiratory disease complex

DOID:3732
hereditary choroidal atrophy

DOID:9794
no_name

DOID:675
toxic megacolon

DOID:1770
TTC21A

http://www.ncbi.nlm.nih.gov/gene/199223
Wolff-Parkinson-White syndrome

HP:0001716
Ocular albinism

HP:0001107
SPG36

http://www.ncbi.nlm.nih.gov/gene/791228
blepharophimosis-intellectual disability syndrome

DOID:0060290
no_name

DOID:8780

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