Annotation Detail
Information
- Associated Genes
- TH
- Associated Variants
-
TH MUTATION
TH MUTATION - Associated Disease
- sudden infant death syndrome
- Source Database
- DisGeNET
- Description
- Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.
- Pubmed
- 24975687
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree,GAD,LHGDN
- DisGENET score for the Gene Disease association
- 0.00563426596522981
Drugs