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.

Muenke Syndrome

ID: DOID:0060703

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

Label: Muenke Syndrome

Synonyms: Muenke Syndrome

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Muenke Syndrome

DOID:0060703
megacystis-microcolon-intestinal hypoperistalsis syndrome

DOID:0060610
dicarboxylic aminoaciduria

DOID:0060650
ulnar-mammary syndrome

DOID:0060614
GALNT16

http://www.ncbi.nlm.nih.gov/gene/57452
RAD51AP2

http://www.ncbi.nlm.nih.gov/gene/729475
ethylmalonic encephalopathy

DOID:0060640
chondrodysplasia-pseudohermaphroditism syndrome

DOID:0060644
hereditary motor and sensory neuropathy with agenesis of the corpus callosum

DOID:0060600
PLPPR3

http://www.ncbi.nlm.nih.gov/gene/79948
KLHL11

http://www.ncbi.nlm.nih.gov/gene/55175
obsolete chronobiology disease

DOID:13364
DNPH1

http://www.ncbi.nlm.nih.gov/gene/10591
cellular myxoid liposarcoma

DOID:5692
papillary follicular thyroid adenocarcinoma

DOID:3968
PHYKPL

http://www.ncbi.nlm.nih.gov/gene/85007
atrophic muscular disease

DOID:913
CHEBI:404748

http://aber-owl.net/drug/CID044391906
resectable bile duct cancer

DOID:5933
obsolete induction by organism of symbiont apoptosis

GO:0052387
B- and T-cell mixed leukemia

DOID:9953
FAM227B

http://www.ncbi.nlm.nih.gov/gene/196951
T-cell adult acute lymphocytic leukemia

DOID:5602
atrioventricular block

DOID:0050820
Kufor-Rakeb syndrome

DOID:0060556
localized extrahepatic bile duct cancer

DOID:5934
OSBPL9

http://www.ncbi.nlm.nih.gov/gene/114883
AIS4

http://www.ncbi.nlm.nih.gov/gene/619405
arteriovenous malformations of the brain

DOID:0060688
Warsaw breakage syndrome

DOID:0060535
germ cell and embryonal cancer

DOID:3095
myeloid dendritic cell antigen processing and presentation

GO:0002469
CHEBI:108194

http://aber-owl.net/drug/CID044267063
RNR1

http://www.ncbi.nlm.nih.gov/gene/6052
Progressive alveolar ridge hypertropy

HP:0009092
IS4

http://www.ncbi.nlm.nih.gov/gene/100190785
LINC01621

http://www.ncbi.nlm.nih.gov/gene/89758
Progressive extrapyramidal muscular rigidity

HP:0007158
obsolete germination

GO:0009844
C7orf26

http://www.ncbi.nlm.nih.gov/gene/79034
primary progressive multiple sclerosis

DOID:0050784
SCA18

http://www.ncbi.nlm.nih.gov/gene/94008
obsolete IMP-GMP specific 5'\''-nucleotidase activity

GO:0017175
LOC100499484-C9ORF174

http://www.ncbi.nlm.nih.gov/gene/57653
TRR-TCT2-1

http://www.ncbi.nlm.nih.gov/gene/7230
ovarian dermoid cyst with prolactin secreting adenoma

DOID:8004
GLC1J

http://www.ncbi.nlm.nih.gov/gene/574078
SLC8B1

http://www.ncbi.nlm.nih.gov/gene/80024
CHEBI:813646

http://aber-owl.net/drug/CID152944320
SureCN7484388

http://aber-owl.net/drug/CID010694630
Myelin tomacula

HP:0030175
S11

http://www.ncbi.nlm.nih.gov/gene/6267
Coccidia infectious disease

DOID:0050244
CHEMBL17666

http://aber-owl.net/drug/CID109957428
PP31-36

http://aber-owl.net/drug/CID013858266
generalized dystonia

DOID:0050835
protein localization to subtelomeric heterochromatin

GO:1903213
obsolete natural killer cell receptor activity

GO:0045233
primary sclerosing cholangitis

DOID:0060643
primary retinal cyst

DOID:12107
CHEBI:259255

http://aber-owl.net/drug/CID044329392
MIR766

http://www.ncbi.nlm.nih.gov/gene/768218
MIR875

http://www.ncbi.nlm.nih.gov/gene/100126309
obsolete negative regulation of Factor XII activation

GO:1905159
Zollinger-Ellison syndrome

DOID:0050782
positive regulation of core promoter binding

GO:1904798
obsolete glypican

GO:0015017
diffuse intraductal papillomatosis

DOID:7444
IGHV3-76

http://www.ncbi.nlm.nih.gov/gene/28406
HLA-DPA2

http://www.ncbi.nlm.nih.gov/gene/646702
cardiac arrest

DOID:0060319
SureCN6638375

http://aber-owl.net/drug/CID118351463
Parabasalia infectious disease

DOID:0050238
RCD1

http://www.ncbi.nlm.nih.gov/gene/5953
D 76

http://aber-owl.net/drug/CID100448997
HEATR5A

http://www.ncbi.nlm.nih.gov/gene/25938
pharyngeal muscle development

GO:0043282
syndrome of infant of a diabetic mother

DOID:14045
CELIAC8

http://www.ncbi.nlm.nih.gov/gene/100188870
urinary tract infiltrating transitional cell carcinoma

DOID:3997
Enlarged proximal interphalangeal joints

HP:0006185
obsolete internalization receptor activity

GO:0015029
CHEBI:363968

http://aber-owl.net/drug/CID044372832
obsolete regulation of transcription involved in G2-phase of mitotic cell cycle

GO:0000116
colorectal adenoma

DOID:0050860
central pterygium

DOID:13473
Asymmetric peripheral demyelination

HP:0030176
psychosexual dysfunction with inhibited sexual excitement

DOID:11954
regulation of systemic arterial blood pressure by aortic body chemoreceptor signaling

GO:0003028
TFPT

http://www.ncbi.nlm.nih.gov/gene/29844
Premature epimetaphyseal fusion in fibula

HP:0012565
recurrent ovarian germ cell neoplasm

DOID:7855
SPD3

http://www.ncbi.nlm.nih.gov/gene/780922
obsolete positive regulation of regulation of insulin secretion involved in cellular response to glucose stimulus

GO:2000530
testicular mixed germ cell-sex cord-stromal neoplasm

DOID:3580
Accessory lunate

HP:0004249
Reticulate pigmentation of oral mucosa

HP:0012788
invasive tubular breast carcinoma

DOID:6587
CELIAC13

http://www.ncbi.nlm.nih.gov/gene/100188875
Premature epimetaphyseal fusion in foot

HP:0012563

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