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.

Urinary excretion of sialylated oligosaccharides

ID: HP:0012061

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

Label: Urinary excretion of sialylated oligosaccharides

Synonyms: Urinary excretion of sialylated oligosaccharides

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Urinary excretion of sialylated oligosaccharides

HP:0012061
Oligosacchariduria

HP:0010471
Increased urinary disaccharide excretion

HP:0012066
Abnormality of proteoglycan metabolism

HP:0004355
Decreased glucosephosphate isomerase activity

HP:0003568
Urinary glycosaminoglycan excretion

HP:0003541
Mucopolysacchariduria

HP:0008155
Abnormal isoelectric focusing of serum transferrin

HP:0003160
Increased serum iduronate sulfatase activity

HP:0003538
Maturity-onset diabetes of the young

HP:0004904
Glycopeptiduria

HP:0012067
Abnormal protein glycosylation

HP:0012346
Abnormality of glycoside metabolism

HP:0003649
Type II transferrin isoform profile

HP:0012301
Increased urinary O-linked sialopeptides

HP:0003461
Abnormal protein N-linked glycosylation

HP:0012347
Abnormality of glycolysis

HP:0004366
Abnormality of polysaccharide metabolism

HP:0011012
Chondroitin sulfate excretion in urine

HP:0012070
Dermatan sulfate excretion in urine

HP:0008301
Aspartylglucosaminuria

HP:0012068
Abnormality of glycoprotein metabolism

HP:0004367
Abnormality of galactoside metabolism

HP:0004342
Increased serum pyruvate

HP:0003542
Type I transferrin isoform profile

HP:0003642
Increased mannosylation of N-linked protein glycosylation

HP:0012357
Keratan sulfate excretion in urine

HP:0012069
Abnormal protein O-linked glycosylation

HP:0012358
Abnormal glycosylation

HP:0012345
Increased sialylation of N-linked protein glycosylation

HP:0012351
Abnormal sialylation of O-linked protein glycosylation

HP:0012362
Reduced activity of N-acetylglucosaminyltransferase II

HP:0003655
Heparan sulfate excretion in urine

HP:0002159
Decreased fucosylation of O-linked protein glycosylation

HP:0012360
Glyoxalase deficiency

HP:0003258
Fibroblast metachromasia

HP:0003610
Decreased mannosylation of N-linked protein glycosylation

HP:0012356
Galactosuria

HP:0012023
Decreased beta-galactosidase activity

HP:0008166
Impairment of fructose metabolism

HP:0011033
Abnormality of glycosaminoglycan metabolism

HP:0004371
Episodic ammonia intoxication

HP:0001951
Decreased sialylation of O-linked protein glycosylation

HP:0012363
Hypergalactosemia

HP:0012024
Abnormal mannosylation of N-linked protein glycosylation

HP:0012355
Decreased fucosylation of N-linked protein glycosylation

HP:0012353
Impairment of galactose metabolism

HP:0004915
Increased C-peptide level

HP:0030796
Abnormal fucosylation of O-linked protein glycosylation

HP:0012359
Hypoketotic hypoglycemia

HP:0001985
Fructose intolerance

HP:0005973
Insulin-dependent but ketosis-resistant diabetes

HP:0008205
Reduced orotidine 5-prime phosphate decarboxylase activity

HP:0003267
Increased fucosylation of N-linked protein glycosylation

HP:0012354
Abnormal sialylation of N-linked protein glycosylation

HP:0012349
Neonatal hypoglycemia

HP:0001998
Decreased sialylation of N-linked protein glycosylation

HP:0012350
Abnormal C-peptide level

HP:0030794
Decreased galactosylation of N-linked protein glycosylation

HP:0012348
Abnormality of vitamin C metabolism

HP:0100509
Galactose intolerance

HP:0004919
Pseudoepiphysis of the proximal phalanx of the 4th toe

HP:0100198
GM2-ganglioside accumulation

HP:0003495
Decreased urinary glucose concentration

HP:0045013
Abnormality of superoxide metabolism

HP:0004358
Reduced C-peptide level

HP:0030795
Molybdenum cofactor deficiency

HP:0003570
Poorly ossified vertebrae

HP:0100856
Ovoid vertebral bodies

HP:0003300
Abnormality of mucopolysaccharide metabolism

HP:0011020
Decreased activity of NADPH oxidase

HP:0003206
Reduced dihydropyrimidine dehydrogenase activity

HP:0003654
Elevated intracellular cystine

HP:0003358
Abnormal fucosylation of protein N-linked glycosylation

HP:0012352
Insulin-resistant diabetes mellitus at puberty

HP:0000877
Decreased CSF biopterin level

HP:0040209
Elevated maternal serum alpha-fetoprotein

HP:0005984
Abnormality of cerebrosidase metabolism

HP:0004344
Absent or minimally ossified vertebral bodies

HP:0004599
Glutathione synthetase deficiency

HP:0003343
Recurrent infantile hypoglycemia

HP:0004914
Decreased activity of mitochondrial complex III

HP:0011924
Increased vertebral height

HP:0004570
Dysostosis multiplex

HP:0000943
Abnormal periosteum morphology

HP:0030313
Vitamin C deficiency

HP:0100510
Glutaric aciduria

HP:0003150
Hypoinsulinemia

HP:0040216
Increased fucosylation of O-linked protein glycosylation

HP:0012361
Ovoid thoracolumbar vertebrae

HP:0003309
Elevated 7-dehydrocholesterol

HP:0010569
gangliosidosis

DOID:2368
Abnormal vertebral ossification

HP:0100569
Unossified vertebral bodies

HP:0004606
Bracket epiphysis of the middle phalanx of the 4th toe

HP:0100181
Triangular shaped middle phalanx of the 2nd toe

HP:0010411
Triangular shaped proximal phalanges of the toes

HP:0010210
Elevated amniotic fluid alpha-fetoprotein

HP:0004639
Cellular metachromasia

HP:0003653
Absent vertebral body mineralization

HP:0004605

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