Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

EVR1

exudative vitreoretinopathy 1 (autosomal dominant! Criswick-Schepens syndrome)FEVR


Gene EVR1 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Amino Acid Sequence

30.0

Chromosomes, Human, Pair 11/*genetics

41.0

Exudates and Transudates

323.0

Female

60.0

Genes, Dominant

20.0

Humans

80.0

Japan

20.0

Male

60.0

Molecular Sequence Data

30.0

Pedigree

60.0

Phenotype

20.0

Proteins/*genetics

30.0

Research Support, Non-U.S. Gov't

80.0

Vitreous Body/*pathology

215.0

Genetic Markers/genetics

20.0

Haplotypes

30.0

Linkage (Genetics)/*genetics

20.0

Eye Diseases, Hereditary/*genetics

210.0

Genes, Dominant/genetics

21.0

Mutation

20.0

Research Support, U.S. Gov't, P.H.S.

30.0

Retinal Diseases/*genetics

26.0

Retinal Diseases/*genetics/pathology

240.0

Chromosome Mapping

20.0

Genetic Markers

20.0

Retinal Vessels/*pathology

220.0