Major Depressive Disorder; Mdd

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Major Depressive Disorder; Mdd

HTR2A
TPH2
FKBP5

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Major Depressive Disorder; Mdd

Neoplasm
Behavioral abnormality
Depressivity
Anxiety
Abnormality of the liver
Stroke
Schizophrenia
Bipolar affective disorder
Alcoholism
Mania

And another 2 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Major Depressive Disorder; Mdd Is also known as unipolar depression.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Major Depressive Disorder; Mdd Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Serotonin Metabolism Deficiency NGS Panel. By Fulgent Genetics Fulgent Genetics (United States). SLC6A4, TPH1, AANAT, TPH2, HTR3C, HTR3E, DDC, HTR1A, HTR1B, HTR2A, HTR2B, HTR2C, HTR3A, HTR3B, HTR5A, HTR6, HTR7 Specificity 12 % Genes 67 %
HTR2A. By Fulgent Genetics Fulgent Genetics (United States). HTR2A Specificity 100 % Genes 34 %
HTR2A. By Genelex (United States). HTR2A Specificity 100 % Genes 34 %
YouScript Psychotropic. By Genelex (United States). SLC6A4, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, HTR2A Specificity 15 % Genes 34 %
GeneSight Psychotropic. By Assurex Health, Inc. (United States). SLC6A4, UGT1A4, UGT2B15, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A4, HLA-A, HTR2A Specificity 10 % Genes 34 %
Comprehensive Pharmacogenomics (PGX) Panel. By ApolloGen, Inc. (United States). SLCO1B1, VKORC1, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, F5, HTR2A, MTHFR, OPRM1 Specificity 10 % Genes 34 %
OneOme RightMed comprehensive test. By OneOme (United States). SLCO1B1, SLC6A4, TPMT, UGT1A1, IFNL3, NUDT15, VKORC1, CYP2B6, CYP2C18, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, F2, F5, GRIK4 , (...) View the complete list with 4 more genes Panel complete gene list SLCO1B1, SLC6A4, TPMT, UGT1A1, IFNL3, NUDT15, VKORC1, CYP2B6, CYP2C18, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, F2, F5, GRIK4, HLA-A, HTR2A, HTR2C, OPRM1 Specificity 5 % Genes 34 %
Citalopram response. By Xcode Life Xcode Life (India). SLC6A4, CYP2C19, HTR2A Specificity 34 % Genes 34 %

You can get up to 5 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10 DEAFNESS, X-LINKED 2; DFNX2 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23 GRACILE BONE DYSPLASIA; GCLEB DIABETES MELLITUS, PERMANENT NEONATAL; PNDM CONE-ROD DYSTROPHY, X-LINKED, 3; CORDX3