Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

DFN2

deafness, X-linked 2, perceptive, congenital


Gene DFN2 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Chromosome Mapping

20.0

Female

30.0

Hearing Loss, Sensorineural/diagnosis/*genetics

212.0

Heterozygote

20.0

Humans

30.0

Linkage (Genetics)

20.0

Male

30.0

Pedigree

20.0