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.

overnutrition

ID: DOID:654

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

Label: overnutrition

Synonyms: overnutrition

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

overnutrition

DOID:654
LOC101927712

http://www.ncbi.nlm.nih.gov/gene/101927712
LINC00917

http://www.ncbi.nlm.nih.gov/gene/732275
PLEKHS1

http://www.ncbi.nlm.nih.gov/gene/79949
MRXS7

http://www.ncbi.nlm.nih.gov/gene/4429
LOC101927414

http://www.ncbi.nlm.nih.gov/gene/101927414
BMIQ7

http://www.ncbi.nlm.nih.gov/gene/404683
RMST

http://www.ncbi.nlm.nih.gov/gene/196475
BP16

http://www.ncbi.nlm.nih.gov/gene/474262
IQCK

http://www.ncbi.nlm.nih.gov/gene/124152
LOC157273

http://www.ncbi.nlm.nih.gov/gene/157273
OR2I1P

http://www.ncbi.nlm.nih.gov/gene/442197
Cardiovascular calcification

HP:0011915
BMIQ8

http://www.ncbi.nlm.nih.gov/gene/56694
LINC02135

http://www.ncbi.nlm.nih.gov/gene/146513
Increased body weight

HP:0004324
Abnormality of the parathyroid physiology

HP:0011767
HOXB-AS3

http://www.ncbi.nlm.nih.gov/gene/404266
kidney failure

DOID:1074
FPGT-TNNI3K

http://www.ncbi.nlm.nih.gov/gene/100526835
AACS

http://www.ncbi.nlm.nih.gov/gene/65985
carbohydrate metabolism disease

DOID:0050013
KCNMA1-AS1

http://www.ncbi.nlm.nih.gov/gene/101929328
FAM185BP

http://www.ncbi.nlm.nih.gov/gene/641808
WAGRO

http://www.ncbi.nlm.nih.gov/gene/100233159
Vascular calcification

HP:0004934
MIR3976HG

http://www.ncbi.nlm.nih.gov/gene/645355
C16orf96

http://www.ncbi.nlm.nih.gov/gene/342346
LINC01500

http://www.ncbi.nlm.nih.gov/gene/102723742
Ectopic calcification

HP:0010766
Abnormal consumption behavior

HP:0040202
Abnormality of body weight

HP:0004323
Abnormality of skeletal physiology

HP:0011843
BECN2

http://www.ncbi.nlm.nih.gov/gene/441925
TTC28-AS1

http://www.ncbi.nlm.nih.gov/gene/284900
BCDIN3D-AS1

http://www.ncbi.nlm.nih.gov/gene/100286844
C8orf34

http://www.ncbi.nlm.nih.gov/gene/116328
Mental deterioration

HP:0001268
Carotid artery dissection

HP:0012158
Abnormality of the cardiovascular system

HP:0001626
Obesity

HP:0001513
bone disease

DOID:0080001
acquired metabolic disease

DOID:0060158
Abnormal eating behavior

HP:0100738
Abnormality of the pituitary gland

HP:0012503
Abnormality of skeletal maturation

HP:0000927
Abnormality of the level of lipoprotein cholesterol

HP:0010979
DSCAM-IT1

http://www.ncbi.nlm.nih.gov/gene/100874326
Dementia

HP:0000726
ZNF608

http://www.ncbi.nlm.nih.gov/gene/57507
TMEM258

http://www.ncbi.nlm.nih.gov/gene/746
Hyperparathyroidism

HP:0000843
Bundle branch block

HP:0011710
Abnormality of acid-base homeostasis

HP:0004360
Abnormality of the endocrine system

HP:0000818
obstructive lung disease

DOID:2320
Abnormality of cholesterol metabolism

HP:0003107
Abnormality of the parathyroid gland

HP:0000828
organ system benign neoplasm

DOID:0060085
Abnormality of bone mineral density

HP:0004348
SureCN1223349

http://aber-owl.net/drug/CID146231719
Abnormality of the nervous system

HP:0000707
Non-Hodgkin lymphoma

HP:0012539
Lymphoma

HP:0002665
Abnormality of long bone morphology

HP:0011314
Abnormality of epiphysis morphology

HP:0005930
nutrition disease

DOID:374
Personality disorder

HP:0012075
Abnormal number of granulocyte precursors

HP:0012137
Abnormality of the upper urinary tract

HP:0010935
thyroid gland disease

DOID:50
Increased susceptibility to fractures

HP:0002659
Medial arterial calcification

HP:0012456
Abnormality of the liver

HP:0001392
Pancreatic islet cell adenoma

HP:0008261
Arthritis

HP:0001369
AMY1B

http://www.ncbi.nlm.nih.gov/gene/277
Abnormality of the basal ganglia

HP:0002134
Abnormal renal morphology

HP:0012210
Renal neoplasm

HP:0009726
Abnormality of glycosphingolipid metabolism

HP:0004343
T-cell lymphoma

HP:0012190
PYY2

http://www.ncbi.nlm.nih.gov/gene/23615
Abnormality of the respiratory system

HP:0002086
MIR522

http://www.ncbi.nlm.nih.gov/gene/574495
Abnormality of the bronchi

HP:0002109
bone osteosarcoma

DOID:3376
Bulimia

HP:0100739
Abnormality of cells of the granulocytic lineage

HP:0012135
PSI associated light-harvesting complex I

GO:0030083
histone H3-K4 demethylation

GO:0034721
lung cancer

DOID:1324
Abdominal obesity

HP:0012743
ventral spinal cord interneuron specification

GO:0021521
CCDC85A

http://www.ncbi.nlm.nih.gov/gene/114800
Abnormality of blood and blood-forming tissues

HP:0001871
Polyphagia

HP:0002591
regulation of myeloid leukocyte differentiation

GO:0002761
Abnormal heart morphology

HP:0001627
EEG with generalized epileptiform discharges

HP:0011198

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