Preferred Name

SOLUTE CARRIER FAMILY 52 (RIBOFLAVIN TRANSPORTER), MEMBER 3

Synonyms

BROWN-VIALETTO-VAN LAERE SYNDROME 1

ID

http://purl.bioontology.org/ontology/OMIM/613350

altLabel

BROWN-VIALETTO-VAN LAERE SYNDROME 1

C20ORF54

FAZIO-LONDE DISEASE

BROWN-VIALETTO-VAN LAERE SYNDROME 1, MILD

RFVT3

RIBOFLAVIN TRANSPORTER 2

CHROMOSOME 20 OPEN READING FRAME 54

SLC52A3

RFT2

cui

C0796274

C0015708

C4017306

C1424064

Gene Locus

20p13

Gene Symbol

C20orf54

RFT2

BVVLS1

SLC52A3

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/613350.0005

http://purl.bioontology.org/ontology/OMIM/613350.0004

http://purl.bioontology.org/ontology/OMIM/613350.0006

http://purl.bioontology.org/ontology/OMIM/613350.0007

http://purl.bioontology.org/ontology/OMIM/613350.0010

http://purl.bioontology.org/ontology/OMIM/613350.0001

http://purl.bioontology.org/ontology/OMIM/613350.0002

http://purl.bioontology.org/ontology/OMIM/613350.0009

http://purl.bioontology.org/ontology/OMIM/613350.0003

http://purl.bioontology.org/ontology/OMIM/613350.0008

MIMTYPEMEANING

Gene with known sequence

notation

613350

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

SOLUTE CARRIER FAMILY 52 (RIBOFLAVIN TRANSPORTER), MEMBER 3

tui

T028

T033

T047

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/PR_000032131 Protein Ontology / 蛋白质本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G12.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/MESH/C537111 Medical Subject Headings / 医学主题词表 CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C191790 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM