Ovarian Dysgenesis 1; Odg1
Description
Hypergonadotropic ovarian failure is a heterogeneous disorder that, in the most severe forms, is a result of ovarian dysgenesis. Ovarian dysgenesis accounts for about half the cases of primary amenorrhea (Timmreck and Reindollar, 2003).
Clinical Features
Top most frequent phenotypes and symptoms related to Ovarian Dysgenesis 1; Odg1
- Hearing impairment
- Neoplasm
- Sensorineural hearing impairment
- Osteoporosis
- Amenorrhea
- Primary amenorrhea
- Clitoral hypertrophy
- Hypoplasia of the uterus
- Secondary amenorrhea
- Gonadal dysgenesis
And another 3 symptoms. If you need more information about this disease we can help you.
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
Ovarian Dysgenesis 1; Odg1 Is also known as gonadal dysgenesis, xx type, xxgd, ovarian dysgenesis, hypergonadotropic, with normal karyotype, ovarian dysgenesis, hypergonadotropic, autosomal recessive, ovarian failure, hypergonadotropic, xx gonadal dysgenesis.
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.Ovarian Dysgenesis 1; Odg1 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Premature Ovarian Failure Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
BMP15, FOXL2, MCM8, PSMC3IP, HFM1, NOBOX, FIGLA, FSHR, LMNA, NR5A1
Specificity
10 %
Genes
100 % |
Premature Ovarian Failure Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
BMP15, FOXL2, MCM8, PSMC3IP, HFM1, NOBOX, FIGLA, FSHR, LMNA, NR5A1
Specificity
10 %
Genes
100 % |
FSHR. Complete sequencing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
FSHR
Specificity
100 %
Genes
100 % |
46,XX gonadal dysgenesis (sequence analysis of FSHR gene).
By CGC Genetics (Portugal).
FSHR
Specificity
100 %
Genes
100 % |
46,XX gonadal dysgenesis (FSH receptor polymorphisms).
By CGC Genetics (Portugal).
FSHR
Specificity
100 %
Genes
100 % |
Ovarian Dysgenesis 1.
By Laboratory of Genetics BioTe21 Adam Master (Poland).
FSHR
Specificity
100 %
Genes
100 % |
Ovarian Dysgenesis and Ovarian Hyperstimulation Syndrome via FSHR Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
FSHR
Specificity
100 %
Genes
100 % |
Female Infertility Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
BMP15, SEMA3A, SEMA3E, FOXL2, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, TAC3, TACR3, WNT4, WT1, WWOX, ZP1, ARL6 , (...)
View the complete list with 84 more genes
Specificity
1 %
Genes
100 % |
You can get up to 19 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MYOPATHY, MYOFIBRILLAR, 8; MFM8 MULTIPLE FIBROADENOMAS OF THE BREAST; MFAB FAMILIAL ADENOMATOUS POLYPOSIS 3; FAP3 DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA; SPAHGC ARGININOSUCCINIC ACIDURIA