Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT)

Alias:
Siddt
Sudden Infant Death-Dysgenesis of the Testes Syndrome
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT), also known as siddt, is related to sudden infant death syndrome and gonadal dysgenesis, and has symptoms including stridor. An important gene associated with Sudden Infant Death with Dysgenesis of the Testes Syndrome is TSPYL1 (TSPY Like 1). Affiliated tissues include testes and spinal cord, and related phenotypes are hypothermia and sleep apnea.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
3
8
2

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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