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Hypertryptophanemia (HYPTRP)

Alias:
Hypertryptophanemia, Familial
Familial Hypertryptophanemia
Hyptrp
[hypertryptophanemia]
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypertryptophanemia, also known as familial hypertryptophanemia, is related to major affective disorder 1 and premature ejaculation. An important gene associated with Hypertryptophanemia is TDO2 (Tryptophan 2,3-Dioxygenase), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. Affiliated tissues include cortex and brain, and related phenotypes are increased serum serotonin and hypertryptophanemia
Related ID：
MALACARDS：HYP187
OMIM：600627
MESH：C563467

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
<1/1000000
14
166
4
HYP187

Medical Symptom

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

Gene & Mutation

#
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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