Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

SEDL

spondyloepiphyseal dysplasia, late


Gene SEDL gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Carrier Proteins/*genetics

80.0

Child

30.0

Humans

210.0

Linkage (Genetics)

40.0

Male

160.0

*Membrane Transport Proteins

152.0

*Mutation

20.0

Osteochondrodysplasias/*genetics

1114.0

X Chromosome

20.0

Adult

60.0

Decompression, Surgical

233.0

Laminectomy

222.0

Tomography, X-Ray Computed

20.0

Animals

40.0

Carrier Proteins/*chemistry

23.0

Comparative Study

20.0

Crystallography, X-Ray

20.0

Mice

20.0

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

140.0

Adolescent

50.0

Child, Preschool

20.0

Female

80.0

Pedigree

100.0

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

50.0

Base Sequence

40.0

Body Height/genetics

218.0

Carrier Proteins/*genetics/metabolism

20.0

DNA Mutational Analysis

30.0

Exons/genetics

40.0

Linkage (Genetics)/*genetics

31.0

Molecular Sequence Data

50.0

Mutation/*genetics

40.0

Phenotype

30.0

RNA, Messenger/analysis/genetics

20.0

X Chromosome/*genetics

30.0

Middle Aged

50.0

Protein Binding

30.0

Protein Structure, Tertiary

20.0

Frameshift Mutation

20.0

Introns/genetics

20.0

Amino Acid Sequence

30.0

Mutation

50.0

Sequence Homology, Amino Acid

30.0

*X Chromosome

40.0

*Linkage (Genetics)

20.0

Recombination, Genetic

20.0

*Codon, Nonsense

23.0

Genetic Diseases, X-Linked/*genetics

314.0

Chromosome Mapping

30.0