Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

PYGM

phosphorylase, glycogen! muscle (McArdle syndrome, glycogen storage disease type V)


Gene PYGM gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Child, Preschool

20.0

Humans

470.0

Female

250.0

Chromosomes, Human, Pair 11/*genetics

72.0

DNA, Neoplasm/genetics

20.0

English Abstract

20.0

Gene Frequency

20.0

*Loss of Heterozygosity

61.0

Microsatellite Repeats

20.0

Chromosomes, Human, Pair 11/genetics

41.0

Gene Deletion

30.0

Multiple Endocrine Neoplasia Type 1/*genetics

129.0

Polymorphism, Genetic

60.0

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

290.0

Adult

130.0

Chromosome Mapping

200.0

Loss of Heterozygosity

30.0

Middle Aged

100.0

Animals

50.0

Base Sequence

130.0

DNA Primers

40.0

*Chromosomes, Human, Pair 11

213.0

Exons

30.0

Genetic Markers

140.0

Male

230.0

Neoplasm Proteins/*genetics

30.0

Polymerase Chain Reaction

180.0

Polymorphism, Single-Stranded Conformational

30.0

*Proto-Oncogene Proteins

30.0

Adolescent

40.0

Phenotype

30.0

Spain

20.0

DNA Mutational Analysis

30.0

*Homozygote

21.0

Mutation, Missense/*genetics

21.0

Polymorphism, Restriction Fragment Length

50.0

Amino Acid Sequence

40.0

Phosphorylases/*genetics

562.0

Adenoma/*genetics

22.0

Aged

50.0

DNA, Neoplasm/analysis

30.0

RNA, Messenger/analysis

20.0

Alleles

40.0

Breast Neoplasms/*genetics/pathology

41.0

Amino Acid Substitution

20.0

Haplotypes

30.0

Multiple Endocrine Neoplasia Type 1/genetics

28.0

Pedigree

120.0

Aged, 80 and over

30.0

Chromosomes, Human, Pair 11

20.0

Linkage (Genetics)

70.0

*Polymorphism, Genetic

30.0

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

30.0

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

90.0

*Chromosome Mapping

50.0

*DNA-Binding Proteins

20.0

Exons/genetics

20.0

Genes/genetics

25.0

Introns/genetics

20.0

Molecular Sequence Data

100.0

Phosphoprotein Phosphatase/*genetics

25.0

Sequence Analysis, DNA

30.0

*Transcription Factors

20.0

Polymorphism, Genetic/genetics

20.0

Transcription, Genetic

20.0

*Chromosome Deletion

60.0

Genes, Tumor Suppressor

30.0

Heterozygote

50.0

*Gene Deletion

30.0

Genetic Markers/genetics

20.0

Carcinoma in Situ/*genetics/pathology

320.0

*Alleles

20.0

Hybrid Cells

30.0

Meiosis

21.0

Eye Proteins/*genetics

21.0

Macular Degeneration/*genetics

24.0

Membrane Proteins/*genetics

20.0

Child

30.0

Recombination, Genetic

30.0

*Mutation

20.0

Blotting, Southern

20.0

Cell Line

20.0

Cricetulus

20.0

Hamsters

20.0

DNA Probes

20.0

*Linkage (Genetics)

30.0

Multiple Endocrine Neoplasia/*genetics

410.0

Muscles/*enzymology

22.0