Body Mass Index Quantitative Trait Locus 9; Bmiq9

Clinical Features

Phenotypes and symptoms related to Body Mass Index Quantitative Trait Locus 9; Bmiq9

  • Obesity

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

Body Mass Index Quantitative Trait Locus 9; Bmiq9 Is also known as obesity, susceptibility to.

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.

Body Mass Index Quantitative Trait Locus 9; Bmiq9 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MC3R. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

MC3R
Specificity
100 %
Genes
100 %
Obesity (sequence analysis of MC3R gene).

By CGC Genetics (Portugal).

MC3R
Specificity
100 %
Genes
100 %
Comprehensive Monogenic Obesity Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

BDNF, SDCCAG8, SIM1, TUB, UCP3, KDM6A, ARL6, RAB23, TRIM32, PHF6, KSR2, IFT27, BBS7, TTC8, MRAP2, IFT74, VPS13B, CPE, CUL4B, BBS10 , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
100 %
Obesity.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München (Germany).

LEP, LEPR, MC3R, MC4R, POMC
Specificity
20 %
Genes
100 %
Obesity, severe, susceptibility to, BMIQ9.

By Praxis fuer Humangenetik Wien (Austria).

MC3R
Specificity
100 %
Genes
100 %
Obesity, severe, susceptibility to, BMIQ9.

By MedGene (Slovakia).

MC3R
Specificity
100 %
Genes
100 %
MC3R.

By Fulgent Genetics Fulgent Genetics (United States).

MC3R
Specificity
100 %
Genes
100 %
Monogenic Obesity Panel.

By Blueprint Genetics (Finland).

SDCCAG8, SIM1, UCP3, ARL6, TRIM32, PHF6, KSR2, BBS7, TTC8, VPS13B, ADCY3, CUL4B, BBS10, BBS12, WDPCP, CEP290, BBS9, DYRK1B, ALMS1, GNAS , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
100 %

You can get up to 4 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MYH7-RELATED LATE-ONSET SCAPULOPERONEAL MUSCULAR DYSTROPHY HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA; HH2 HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA; HTC3 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY DENYS-DRASH SYNDROME; DDS EHLERS-DANLOS SYNDROME TYPE 7A MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB