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.

ethylmalonic encephalopathy

ID: DOID:0060640

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

Label: ethylmalonic encephalopathy

Synonyms: ethylmalonic encephalopathy

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

ethylmalonic encephalopathy

DOID:0060640
hereditary motor and sensory neuropathy with agenesis of the corpus callosum

DOID:0060600
Muenke Syndrome

DOID:0060703
megacystis-microcolon-intestinal hypoperistalsis syndrome

DOID:0060610
ulnar-mammary syndrome

DOID:0060614
dicarboxylic aminoaciduria

DOID:0060650
obsolete chronobiology disease

DOID:13364
papillary follicular thyroid adenocarcinoma

DOID:3968
PLPPR3

http://www.ncbi.nlm.nih.gov/gene/79948
GLC1J

http://www.ncbi.nlm.nih.gov/gene/574078
arteriovenous malformations of the brain

DOID:0060688
atrophic muscular disease

DOID:913
pyruvate carboxylase deficiency disease

DOID:3651
RAD51AP2

http://www.ncbi.nlm.nih.gov/gene/729475
TRR-TCT2-1

http://www.ncbi.nlm.nih.gov/gene/7230
KLHL11

http://www.ncbi.nlm.nih.gov/gene/55175
GALNT16

http://www.ncbi.nlm.nih.gov/gene/57452
omphalocele

DOID:0060327
eye carcinoma in situ

DOID:8792
atrioventricular block

DOID:0050820
OSBPL9

http://www.ncbi.nlm.nih.gov/gene/114883
cytochrome-c oxidase deficiency disease

DOID:3762
mitochondrial metabolism disease

DOID:700
primary progressive multiple sclerosis

DOID:0050784
HLA-DPA2

http://www.ncbi.nlm.nih.gov/gene/646702
chondrodysplasia-pseudohermaphroditism syndrome

DOID:0060644
AIS4

http://www.ncbi.nlm.nih.gov/gene/619405
IS4

http://www.ncbi.nlm.nih.gov/gene/100190785
mitochondrial complex I deficiency

DOID:0060536
collagenous colitis

DOID:0060183
RCD1

http://www.ncbi.nlm.nih.gov/gene/5953
B- and T-cell mixed leukemia

DOID:9953
primary sclerosing cholangitis

DOID:0060643
LOC100499484-C9ORF174

http://www.ncbi.nlm.nih.gov/gene/57653
T-cell adult acute lymphocytic leukemia

DOID:5602
Kufor-Rakeb syndrome

DOID:0060556
cellular myxoid liposarcoma

DOID:5692
SureCN1043722

http://aber-owl.net/drug/CID044438556
cardiac arrest

DOID:0060319
pseudohermaphroditism

DOID:3765
CHEMBL1911709

http://aber-owl.net/drug/CID057396259
FAM117A

http://www.ncbi.nlm.nih.gov/gene/81558
RNR1

http://www.ncbi.nlm.nih.gov/gene/6052
S11

http://www.ncbi.nlm.nih.gov/gene/6267
sensory peripheral neuropathy

DOID:2491
ectopic pregnancy

DOID:0060329
LINC01621

http://www.ncbi.nlm.nih.gov/gene/89758
SPD3

http://www.ncbi.nlm.nih.gov/gene/780922
LOAS

http://www.ncbi.nlm.nih.gov/gene/100188775
Leigh disease

DOID:3652
urea cycle disorder

DOID:9267
MIR766

http://www.ncbi.nlm.nih.gov/gene/768218
carbodiimide

http://aber-owl.net/drug/CID100009864
JAKMIP1

http://www.ncbi.nlm.nih.gov/gene/152789
phenylketonuria

DOID:9281
GLC1H

http://www.ncbi.nlm.nih.gov/gene/399564
purine nucleoside phosphorylase deficiency

DOID:5813
HTOR

http://www.ncbi.nlm.nih.gov/gene/3349
Nance-Horan syndrome

DOID:0060599
MYP10

http://www.ncbi.nlm.nih.gov/gene/553195
Zollinger-Ellison syndrome

DOID:0050782
BSPT salt

http://aber-owl.net/drug/CID006105620
no_name

GO:0048552
cyclic hematopoiesis

DOID:5339
myelomeningocele

DOID:0060326
germ cell and embryonal cancer

DOID:3095
lactic acidosis

DOID:3650
PDB4

http://www.ncbi.nlm.nih.gov/gene/94003
esophagus small cell carcinoma

DOID:7134
GS-HNE

http://aber-owl.net/drug/CID005460851
NHSL1

http://www.ncbi.nlm.nih.gov/gene/57224
renal glycosuria

DOID:9432
Warsaw breakage syndrome

DOID:0060535
maple syrup urine disease

DOID:9269
mucosulfatidosis

DOID:0050441
CHEBI:817103

http://aber-owl.net/drug/CID011649854
fructose-1,6-bisphosphatase deficiency

DOID:5204
colorectal adenoma

DOID:0050860
C7orf26

http://www.ncbi.nlm.nih.gov/gene/79034
axonal neuropathy

DOID:7319
gingivitis

DOID:3087
Menkes disease

DOID:1838
coagulation protein disease

DOID:2212
ablepharon macrostomia syndrome

DOID:0060550
DEFB107A

http://www.ncbi.nlm.nih.gov/gene/245910
TFPT

http://www.ncbi.nlm.nih.gov/gene/29844
ornithine carbamoyltransferase deficiency

DOID:9271
MADAM dihydrochloride

http://aber-owl.net/drug/CID110084648
primary hyperoxaluria

DOID:2977
ERICH3

http://www.ncbi.nlm.nih.gov/gene/127254
acute intermittent porphyria

DOID:3890
parasitic helminthiasis infectious disease

DOID:883
prion disease

DOID:649
central core myopathy

DOID:3529
ischemic colitis

DOID:0060181
DNPH1

http://www.ncbi.nlm.nih.gov/gene/10591
LOC401478

http://www.ncbi.nlm.nih.gov/gene/401478
HEATR5A

http://www.ncbi.nlm.nih.gov/gene/25938
prediabetes syndrome

DOID:11716
AFAP1-AS1

http://www.ncbi.nlm.nih.gov/gene/84740

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