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.

mitochondrial complex III deficiency nuclear type 1

ID: DOID:0080111

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

Label: mitochondrial complex III deficiency nuclear type 1

Synonyms: mitochondrial complex III deficiency nuclear type 1

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

mitochondrial complex III deficiency nuclear type 1

DOID:0080111
mitochondrial complex III deficiency nuclear type 3

DOID:0080112
mitochondrial complex III deficiency nuclear type 8

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mitochondrial DNA depletion syndrome 8a

DOID:0080127
mitochondrial DNA depletion syndrome 3

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mitochondrial complex III deficiency nuclear type 4

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mitochondrial DNA depletion syndrome 9

DOID:0080128
mitochondrial DNA depletion syndrome 1

DOID:0080119
mitochondrial DNA depletion syndrome 2

DOID:0080120
mitochondrial complex III deficiency nuclear type 7

DOID:0080116
mitochondrial complex III deficiency nuclear type 6

DOID:0080115
multiple mitochondrial dysfunctions syndrome 3

DOID:0080135
multiple mitochondrial dysfunctions syndrome 4

DOID:0080136
coenzyme Q10 deficiency disease

DOID:0050730
mitochondrial DNA depletion syndrome 7

DOID:0080126
mitochondrial DNA depletion syndrome 12

DOID:0080130
mitochondrial DNA depletion syndrome 5

DOID:0080124
mitochondrial DNA depletion syndrome 6

DOID:0080125
mitochondrial DNA depletion syndrome 4a

DOID:0080122
mitochondrial DNA depletion syndrome 13

DOID:0080131
mitochondrial DNA depletion syndrome 11

DOID:0080129
multiple mitochondrial dysfunctions syndrome 1

DOID:0080133
mitochondrial complex III deficiency nuclear type 9

DOID:0080118
mitochondrial complex III deficiency nuclear type 2

DOID:0060351
mitochondrial complex III deficiency nuclear type 5

DOID:0080114
Sengers syndrome

DOID:0080132
multiple mitochondrial dysfunctions syndrome 2

DOID:0080134
mitochondrial DNA depletion syndrome 4b

DOID:0080123
vitamin metabolic disorder

DOID:0050718
Decreased CSF amyloid level

HP:0030861
cerebral folate receptor alpha deficiency

DOID:0050719
obsolete modulation by organism of symbiont resistance gene-dependent defense response

GO:0052466
lung clear cell-sugar-tumor

DOID:5763
Trichophyton schoenleinii tinea capitis

DOID:0050110
disorder of optic chiasm associated with inflammatory disorder

DOID:12651
Hyperoxaluria

HP:0003159
regulation of apoptosis involved in tissue homeostasis

GO:0060785
obsolete 4-toluenecarboxylate biosynthetic process

GO:0046270
mitochondrial complex II deficiency

DOID:0060537
codeinone reductase (NADPH) activity

GO:0047036
Hypoautofluorescent macular lesion

HP:0030632
obsolete protein tetramerization activity

GO:0051074
mitochondrial metabolism disease

DOID:700
obsolete SAP kinase 3 activity

GO:0016910
ileal disease

DOID:11606
orotic aciduria

DOID:0050833
apoptotic process involved in atrial ventricular junction remodeling

GO:0003296
Abnormal CSF dopamine level

HP:0012654
neuroblast fate determination

GO:0007400
Hodgkin'\''s paragranuloma involving lymph nodes of multiple sites

DOID:9079
PHGDH deficiency

DOID:0050722
obsolete signal transmission via diffusible molecule

GO:0023017
senile degeneration of brain

DOID:14524
adenocarcinoma in adenomatous polyposis coli

DOID:8269
Type A brachydactyly

HP:0009370
no_name

GO:0005453
sugar-terminal-phosphatase activity

GO:0050309
contact dermatitis due to arnica

DOID:4410
macrocystic neurilemmoma

DOID:3203
Reduced CSF dopamine level

HP:0012656
no_name

DOID:11392
ganglion mother cell fate determination

GO:0007402
Cystinuria

HP:0003131
Megaloblastic anemia

HP:0001889
congenital chromosomal disease

DOID:1086
uterine corpus myxoid leiomyoma

DOID:13956
regulation of nuclear-transcribed mRNA catabolic process

GO:2000622
uterine corpus epithelioid leiomyoma

DOID:13951
apoptotic process involved in endocardial cushion morphogenesis

GO:0003277
gap junction channel activity involved in cardiac conduction electrical coupling

GO:0086075
glycogen storage disease XV

DOID:0050579
obsolete small monomeric GTPase activity

GO:0003925
pyrimidine metabolic disorder

DOID:0050832
protein localization to linear element

GO:0036181
diversion colitis

DOID:0060187
childhood central nervous system mixed germ cell tumor

DOID:7516
Abnormality of cysteine metabolism

HP:0010918
uterine corpus lipoleiomyoma

DOID:13957
gap junction channel activity involved in atrial cardiac muscle cell-AV node cell electrical coupling

GO:0086076
Clostridium difficile colitis

DOID:0060185
obsolete modulation by organism of symbiont inflammatory response

GO:0052451
regulation of metanephros development

GO:0072215
obsolete bacterial-type ferredoxin

GO:0009498
Mild expressive language delay

HP:0011346
regulation of ribosomal large subunit export from nucleus

GO:2000203
ERBB4 signaling pathway

GO:0038130
apoptotic process involved in metanephric collecting duct development

GO:1900204
CHEBI:496223

http://aber-owl.net/drug/CID144431700
obsolete regulation of initiation of T cell receptor signaling

GO:0023010
obsolete matrilysin activity

GO:0004235
no_name

DOID:9845
obsolete secretin (sensu Bacteria)

GO:0015480
obsolete regulation of histone modification by regulation of transcription from RNA polymerase II promoter

GO:1900410
mitochondrial complex I deficiency

DOID:0060536
Lytic defects of humeral diaphysis

HP:0003930
anaplastic renal Wilms'\'' tumor

DOID:5185
lipoma of intra-abdominal organ

DOID:10204
pulmonary type ovarian small cell carcinoma

DOID:7650
obsolete Palpitations (with pheochromocytoma)

HP:0001676
protein localization to chloroplast

GO:0072598

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