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.

non-syndromic intellectual disability

ID: DOID:0050889

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

Label: non-syndromic intellectual disability

Synonyms: non-syndromic intellectual disability

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

non-syndromic intellectual disability

DOID:0050889
syndromic intellectual disability

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autosomal recessive non-syndromic intellectual disability

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autosomal dominant non-syndromic intellectual disability

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Stormorken syndrome

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syndromic X-linked intellectual disability

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Scheie syndrome

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pontocerebellar hypoplasia type 1B

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agnathia-otocephaly complex

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spastic ataxia 2

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chromosomal duplication syndrome

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chromosome 22q11.2 deletion syndrome

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hereditary hypophosphatemic rickets with hypercalciuria

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chromosome 17p13.3 duplication syndrome

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autosomal recessive early-onset Parkinson disease 7

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orofaciodigital syndrome V

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chromosome 2p16.1-p15 deletion syndrome

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Renpenning syndrome

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branchiootic syndrome

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chromosome 4q21 deletion syndrome

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chromosome 22q11.2 microduplication syndrome

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Mast syndrome

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non-syndromic X-linked intellectual disability

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chromosome 1p36 deletion syndrome

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orofaciodigital syndrome XI

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autosomal dominant Parkinson disease 1

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amyotrohpic lateral sclerosis type 22

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Kleefstra syndrome

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cardiofaciocutaneous syndrome

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chromosome Xp21 deletion syndrome

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chromosome 1q21.1 duplication syndrome

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photosensitive epilepsy

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chromosome 15q24 deletion syndrome

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autosomal dominant Parkinson disease 8

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choreatic disease

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chromosome 14q11-q22 deletion syndrome

DOID:0060392
3MC syndrome 3

DOID:0060577
3p- syndrome

DOID:0060417
chromosome 22q13 duplication syndrome

DOID:0060437
congenital fiber-type disproportion

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Van Maldergem syndrome

DOID:0060238
muscular dystrophy-dystroglycanopathy

DOID:0050588
MEDNIK syndrome

DOID:0060483
idiopathic scoliosis

DOID:0060250
iridogoniodysgenesis syndrome

DOID:0050786
chromosome 15q11.2 deletion syndrome

DOID:0060393
fibrochondrogenesis

DOID:0060465
orofaciodigital syndrome IX

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chromosome 3q29 microduplication syndrome

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Hallermann-Streiff syndrome

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chromosome 5p13 duplication syndrome

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chromosome 13q14 deletion syndrome

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congenital myopathy

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proximal symphalangism

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amyotrophic lateral sclerosis type 4

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short chain acyl-CoA dehydrogenase deficiency

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orofaciodigital syndrome IV

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acrofacial dysostosis

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Desbuquois dysplasia

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orofaciodigital syndrome III

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chromosome 18q deletion syndrome

DOID:0060407
Feingold syndrome

DOID:0060464
chromosome 3q13.31 deletion syndrome

DOID:0060418
chromosome 15q13.3 microdeletion syndrome

DOID:0060394
chromosome 16p13.3 duplication syndrome

DOID:0060431
orofaciodigital syndrome VIII

DOID:0060378
very long chain acyl-CoA dehydrogenase deficiency

DOID:0080155
chromosome 18p deletion syndrome

DOID:0060406
spastic ataxia 3

DOID:0050942
chromosome 19p13.13 deletion syndrome

DOID:0060426
dyschromatosis universalis hereditaria

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chromosome 6pter-p24 deletion syndrome

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synpolydactyly

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multiple pterygium syndrome

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Armfield syndrome

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chromosome 1q21.1 deletion syndrome

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autosomal recessive juvenile Parkinson disease 2

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chromosomal deletion syndrome

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pontocerebellar hypoplasia type 7

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autosomal recessive early-onset Parkinson disease 15

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oculoauricular syndrome

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medium chain acyl-CoA dehydrogenase deficiency

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pontocerebellar hypoplasia type 2C

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spastic quadriplegia

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pontocerebellar hypoplasia type 3

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orofaciodigital syndrome VII

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chromosome 17q12 deletion syndrome

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3MC syndrome

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distal 10q deletion syndrome

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fetal valproate syndrome

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autosomal recessive hypophosphatemic rickets

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Joubert syndrome with orofaciodigital defect

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pontocerebellar hypoplasia type 2A

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multiple synostoses syndrome

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CLAM

http://www.ncbi.nlm.nih.gov/gene/373073
orofaciodigital syndrome X

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autosomal dominant chondrodysplasia punctata

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Ogden syndrome

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chromosome 16p11.2 deletion syndrome

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Koolen de Vries syndrome

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