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.

Borjeson-Forssman-Lehmann syndrome

ID: DOID:0050681

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

Label: Borjeson-Forssman-Lehmann syndrome

Synonyms: Borjeson-Forssman-Lehmann syndrome

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Borjeson-Forssman-Lehmann syndrome

DOID:0050681
Aicardi syndrome

DOID:8461
non-syndromic X-linked intellectual disability

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IDSP1

http://www.ncbi.nlm.nih.gov/gene/3424
Goldenhar syndrome

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orofaciodigital syndrome

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mucopolysaccharidosis II

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Cri-Du-Chat syndrome

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FG syndrome

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FGS3

http://www.ncbi.nlm.nih.gov/gene/93985
oculocerebrorenal syndrome

DOID:1056
periventricular nodular heterotopia

DOID:0050454
Simpson-Golabi-Behmel syndrome

DOID:0060248
WTRS

http://www.ncbi.nlm.nih.gov/gene/619509
red-green color blindness

DOID:13909
Ogden syndrome

DOID:0050781
Axenfeld-Rieger syndrome

DOID:14686
Renpenning syndrome

DOID:0060179
centronuclear myopathy

DOID:14717
Allan-Herndon-Dudley syndrome

DOID:0050631
AIC

http://www.ncbi.nlm.nih.gov/gene/192
X-linked nonsyndromic deafness

DOID:0050566
HPE8

http://www.ncbi.nlm.nih.gov/gene/619406
holoprosencephaly

DOID:4621
C4orf48

http://www.ncbi.nlm.nih.gov/gene/401115
Wolf-Hirschhorn syndrome

DOID:0050460
autosomal recessive nonsyndromic deafness

DOID:0050565
focal dermal hypoplasia

DOID:2120
Kennedy'\''s disease

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mucopolysaccharidosis

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nemaline myopathy

DOID:3191
spastic quadriplegia

DOID:10970
orofaciodigital syndrome XI

DOID:0060381
Cornelia de Lange syndrome

DOID:11725
Klippel-Feil syndrome

DOID:10426
amyotrohpic lateral sclerosis type 22

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Leber hereditary optic neuropathy

DOID:705
Scheie syndrome

DOID:0060222
fragile X syndrome

DOID:14261
branchiootorenal syndrome

DOID:14702
Boomerang dysplasia

DOID:0050680
hyperostosis frontalis interna

DOID:9925
autosomal dominant microcephaly

DOID:14725
malignant glandular tumor of peripheral nerve sheath

DOID:8420
WBS2

http://www.ncbi.nlm.nih.gov/gene/7457
PRBNS

http://www.ncbi.nlm.nih.gov/gene/100301572
pituitary hypoplasia

DOID:7378
optic atrophy

DOID:5723
metachromatic leukodystrophy

DOID:10581
Waardenburg'\''s syndrome

DOID:9258
Dent disease

DOID:0050699
Sakati-Nyhan syndrome

DOID:0060359
ZIC4

http://www.ncbi.nlm.nih.gov/gene/84107
partial optic atrophy

DOID:10631
inhibited male orgasm

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CSAG3

http://www.ncbi.nlm.nih.gov/gene/389903
Noonan syndrome

DOID:3490
CHRD

http://www.ncbi.nlm.nih.gov/gene/8646
MTMR1

http://www.ncbi.nlm.nih.gov/gene/8776
bluetongue

DOID:1335
persistent hyperplastic primary vitreous

DOID:0060282
WHCR

http://www.ncbi.nlm.nih.gov/gene/7467
Hypoplasia of the antihelix

HP:0009739
coloboma of optic nerve

DOID:11975
Waterhouse-Friderichsen syndrome

DOID:9931
mumps

DOID:10264
EYA2

http://www.ncbi.nlm.nih.gov/gene/2139
bradyopsia

DOID:0050335
IKBKGP1

http://www.ncbi.nlm.nih.gov/gene/246210
LOAS

http://www.ncbi.nlm.nih.gov/gene/100188775
Aarskog syndrome

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chondrodysplasia punctata

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non-syndromic intellectual disability

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Vici syndrome

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osteogenesis imperfecta

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Partington syndrome

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46 XX gonadal dysgenesis

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extragonadal nonseminomatous germ cell tumor

DOID:5677
TRAPPC2B

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DWS

http://www.ncbi.nlm.nih.gov/gene/1858
LINC00893

http://www.ncbi.nlm.nih.gov/gene/100131434
renal glycosuria

DOID:9432
BRWD3

http://www.ncbi.nlm.nih.gov/gene/254065
Loeys-Dietz syndrome

DOID:0050466
mucopolysaccharidosis VI

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NXT2

http://www.ncbi.nlm.nih.gov/gene/55916
congenital muscular dystrophy

DOID:0050557
no_name

http://www.ncbi.nlm.nih.gov/gene/8197
autosomal recessive juvenile Parkinson disease 2

DOID:0060368
HTC2

http://www.ncbi.nlm.nih.gov/gene/3342
brain compression

DOID:11457
X-linked disease

DOID:0050735
salpingitis isthmica nodosa

DOID:5730
craniometaphyseal dysplasia

DOID:0080033
KBG syndrome

DOID:14780
Weissenbacher-Zweymuller syndrome

DOID:4258
microphthalmia

DOID:10629
Balo concentric sclerosis

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FGS2

http://www.ncbi.nlm.nih.gov/gene/2270
rhizomelic chondrodysplasia punctata

DOID:2580

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