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.

SCZD12

ID: http://www.ncbi.nlm.nih.gov/gene/619488

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

Label: SCZD12

Synonyms: SCZD12, schizophrenia 12, schizophrenia susceptibility locus, chromosome 1p-related

Alternative IDs: 619488

API: GO

SPARQL: GO

Similar Entities

SCZD12

http://www.ncbi.nlm.nih.gov/gene/619488
velocardiofacial syndrome

DOID:12583
LOC102724770

http://www.ncbi.nlm.nih.gov/gene/102724770
CECR7

http://www.ncbi.nlm.nih.gov/gene/100130418
DGS2

http://www.ncbi.nlm.nih.gov/gene/8026
acrocephalosyndactylia

DOID:12960
thrombocytopenia-absent radius syndrome

DOID:14699
SMA5

http://www.ncbi.nlm.nih.gov/gene/11042
acromesomelic dysplasia

DOID:0080052
Absent forearm bone

HP:0003953
radioulnar synostosis

DOID:9827
Roberts syndrome

DOID:5325
Aplasia/hypoplasia of the humerus

HP:0006507
GSC2

http://www.ncbi.nlm.nih.gov/gene/2928
Rubinstein-Taybi syndrome

DOID:1933
Abnormality of the femoral head

HP:0003368
synostosis

DOID:11971
Unilateral radial aplasia

HP:0011908
Abnormality of the femoral neck

HP:0003367
Abnormality of the femoral neck or head region

HP:0003366
Acromelia of the upper limbs

HP:0010482
VACTERL association

DOID:14679
Aplasia/hypoplasia involving forearm bones

HP:0006503
Absent humerus

HP:0003862
CHEMBL2048784

http://aber-owl.net/drug/CID157412596
Absent radius

HP:0003974
TBC1D32

http://www.ncbi.nlm.nih.gov/gene/221322
mucopolysaccharidosis II

DOID:12799
Pointed proximal second through fifth metacarpals

HP:0001223
Saethre-Chotzen syndrome

DOID:14768
chromosomal deletion syndrome

DOID:0060388
DiGeorge syndrome

DOID:11198
bone development disease

DOID:0080006
Acromelia of the lower limbs

HP:0010494
CHEBI:403944

http://aber-owl.net/drug/CID144391373
CHEBI:468678

http://aber-owl.net/drug/CID044419959
Flattened femoral head

HP:0008812
Aplasia/Hypoplasia of the radius

HP:0006501
Silver-Russell syndrome

DOID:14681
Abnormality of upper limb bone

HP:0040070
Aplasia involving forearm bones

HP:0009822
Aplasia/hypoplasia involving bones of the extremities

HP:0045060
acrofacial dysostosis

DOID:0060379
Aplasia/hypoplasia involving bones of the upper limbs

HP:0006496
no_name

DOID:14713
Forearm undergrowth

HP:0009821
Acromelia

HP:0010884
Abnormality of the upper arm

HP:0001454
Acromesomelia

HP:0003086
Humerus varus

HP:0003874
chondrodysplasia-pseudohermaphroditism syndrome

DOID:0060644
Abnormality of limb bone

HP:0040068
progeria

DOID:3911
IDSP1

http://www.ncbi.nlm.nih.gov/gene/3424
brachydactyly

DOID:0050581
Greig cephalopolysyndactyly syndrome

DOID:14761
Y-shaped metacarpals

HP:0006042
Hypoplastic distal humeri

HP:0005025
SureCN3806770

http://aber-owl.net/drug/CID046225507
no_name

DOID:0080004
Abnormal morphology of forearm bone

HP:0040073
no_name

DOID:9871
cutaneous mastocytosis

DOID:3663
SPPM

http://www.ncbi.nlm.nih.gov/gene/8090
Amelia involving the upper limbs

HP:0009812
Short metacarpals with rounded proximal ends

HP:0006161
Aplasia/hypoplasia of the extremities

HP:0009815
LINC00893

http://www.ncbi.nlm.nih.gov/gene/100131434
Cuboidal metacarpal

HP:0006011
Abnormal morphology of bones of the upper limbs

HP:0040065
IGHD1-7

http://www.ncbi.nlm.nih.gov/gene/28509
SC phocomelia syndrome

DOID:0050536
CHEBI:810082

http://aber-owl.net/drug/CID152943276
Amelia involving the lower limbs

HP:0009818
Long ulna

HP:0003988
DFNA7

http://www.ncbi.nlm.nih.gov/gene/1689
dental enamel hypoplasia

DOID:693
Small finger

HP:0030033
endosteal hyperostosis

DOID:0080034
autosomal dominant microcephaly

DOID:14725
Broad metacarpals

HP:0001230
no_name

DOID:9242
TNFSF12-TNFSF13

http://www.ncbi.nlm.nih.gov/gene/407977
CHEBI:733890

http://aber-owl.net/drug/CID146891582
Short humerus

HP:0005792
INPP5B

http://www.ncbi.nlm.nih.gov/gene/3633
TLDC1

http://www.ncbi.nlm.nih.gov/gene/57707
Upper limb undergrowth

HP:0009824
Legg-Calve-Perthes disease

DOID:14415
Short 5th toe

HP:0011917
hypophosphatemia

DOID:0050336
cleidocranial dysplasia

DOID:13994
Aplasia/Hypoplasia involving the femoral head and neck

HP:0009108
polydactyly

DOID:1148
Abnormality of limb bone morphology

HP:0002813
Slender metacarpals

HP:0006236
Velopharyngeal insufficiency

HP:0000220
syndactyly

DOID:11193
DFNX3

http://www.ncbi.nlm.nih.gov/gene/1680
CHEBI:782795

http://aber-owl.net/drug/CID149862117

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