Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

IDDM2

insulin-dependent diabetes mellitus 2


Gene IDDM2 gene interaction
View Neighborhood Gene

Result number fewer <<<< << < ALL > >> >>> more

MeSH term
FrequencyCondition_Probility

Comparative Study

30.0

Genetic Predisposition to Disease/*genetics

41.0

Humans

500.0

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

440.0

Adolescent

90.0

Child

90.0

Diabetes Mellitus, Type 1/*genetics

3617.0

Female

180.0

*Genomic Imprinting

20.0

Insulin/*genetics

1727.0

Insulin-Like Growth Factor II/*genetics

42.0

Male

180.0

Sex Factors

20.0

Adult

100.0

Age of Onset

20.0

Diabetes Mellitus, Type 1/epidemiology/*genetics

418.0

Genome, Human

40.0

Genotype

130.0

HLA Antigens/genetics

30.0

Linkage (Genetics)/*genetics

20.0

Lod Score

30.0

Nuclear Family

20.0

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

110.0

Alleles

190.0

Base Sequence

40.0

Diabetes Mellitus, Type 2/genetics

24.0

*Genetic Predisposition to Disease

50.0

*Minisatellite Repeats

56.0

Molecular Sequence Data

60.0

Polymerase Chain Reaction

50.0

*Polymorphism, Genetic

40.0

Animals

100.0

Chromosome Mapping

110.0

Crosses, Genetic

20.0

Rats

20.0

Insulin/genetics

516.0

Diabetes Mellitus, Type 1/*genetics/immunology

35.0

Genetic Markers

50.0

HLA Antigens/*genetics

30.0

HLA-DQ Antigens/genetics

51.0

HLA-DR Antigens/genetics

41.0

Genetic Predisposition to Disease

120.0

Haplotypes

60.0

Major Histocompatibility Complex/genetics

35.0

Polymorphism, Genetic

80.0

Risk Factors

30.0

Time Factors

20.0

Minisatellite Repeats/*genetics

34.0

Genetic Predisposition to Disease/genetics

30.0

*Transcription, Genetic

20.0

Diabetes Mellitus, Type 1/epidemiology/*etiology/genetics

2100.0

Major Histocompatibility Complex

20.0

*Chromosome Mapping

40.0

Chromosomes, Human, Pair 11

41.0

Minisatellite Repeats

96.0

*Alleles

20.0

Chromosomes, Human, Pair 6

21.0

Fathers

23.0

*Linkage (Genetics)

50.0

Mothers

22.0

Pedigree

30.0

Variation (Genetics)

50.0

Middle Aged

20.0

Gene Frequency

40.0

*Gene Expression

20.0

Polymorphism, Restriction Fragment Length

30.0

Genes

20.0

Incidence

30.0

Disease Susceptibility

70.0

Polymorphism, Genetic/genetics

20.0

Case-Control Studies

30.0

Child, Preschool

60.0

*Immunoconjugates

20.0

Infant

40.0

Genome

20.0

Mice

40.0

*Chromosomes, Human, Pair 11

20.0

DNA Primers

20.0

Insulin/*biosynthesis/*genetics

250.0

RNA, Messenger/biosynthesis

20.0

Graves' Disease/genetics

225.0

Gene Expression

20.0

Haplotypes/genetics

20.0

Insulin-Like Growth Factor II/genetics

22.0

European Continental Ancestry Group

20.0

Risk Assessment

20.0

Finland

20.0

Polymorphism, Single Nucleotide/genetics

20.0

Linkage (Genetics)

30.0

Genomic Imprinting

21.0

Linkage Disequilibrium

20.0

Mice, Inbred NOD

20.0

DNA, Satellite/genetics

21.0

Genetic Screening

20.0