Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

SHOX

short stature homeoboxPHOG


Gene SHOX gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Adult

90.0

Aged

20.0

Child

150.0

DNA Mutational Analysis

30.0

Female

270.0

Gene Deletion

50.0

Homeodomain Proteins/*genetics/metabolism

22.0

Humans

370.0

Male

210.0

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

40.0

Base Sequence

40.0

Genotype

40.0

Haplotypes

20.0

Heterozygote

20.0

Homeodomain Proteins/*genetics

235.0

Mutation

60.0

Recombination, Genetic

20.0

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

230.0

X Chromosome/*genetics

51.0

Adolescent

100.0

Body Height/*genetics

1242.0

Dosage Compensation (Genetics)

21.0

Estrogen Replacement Therapy

24.0

In Situ Hybridization, Fluorescence

90.0

Child, Preschool

60.0

Homeodomain Proteins/genetics

73.0

*Gene Deletion

60.0

Prevalence

20.0

Karyotyping

60.0

Polymerase Chain Reaction

40.0

Polymorphism, Single-Stranded Conformational

30.0

Sequence Analysis, DNA

20.0

Translocation, Genetic

30.0

Turner Syndrome/genetics

333.0

Blotting, Southern

20.0

*Genes, Homeobox

62.0

Osteochondrodysplasias/*genetics

33.0

Phenotype

80.0

Syndrome

60.0

Chromosome Aberrations

20.0

Body Height

31.0

Genetic Screening

20.0

Infant, Newborn

30.0

*Chromosome Deletion

20.0

Chromosome Mapping

20.0

Chromosome Banding

20.0

Chromosome Painting

24.0

Family Health

30.0

Cloning, Molecular

20.0

Growth Disorders/*genetics

712.0

Hormones/blood

21.0

X Chromosome

40.0

Y Chromosome

33.0

Immunohistochemistry

20.0

Amino Acid Sequence

30.0

Molecular Sequence Data

50.0

*Mutation

50.0

*Protein-Tyrosine Kinase

20.0

Receptors, Fibroblast Growth Factor/genetics

23.0

Turner Syndrome/*genetics

314.0

Bone and Bones/*abnormalities

29.0

Pedigree

110.0

Linkage (Genetics)

20.0

Lod Score

20.0

Pregnancy

20.0

Cohort Studies

20.0

Growth/*genetics

228.0

Growth Disorders/genetics

26.0