Spermatogenic Failure 17; Spgf17
Clinical Features
Phenotypes and symptoms related to Spermatogenic Failure 17; Spgf17
- Infertility
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
Spermatogenic Failure 17; Spgf17 Is also known as male infertility due to oocyte activation failure.
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.Spermatogenic Failure 17; Spgf17 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Male Infertility Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SEMA3A, SEMA3E, FOXL2, BRDT, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAR, AURKC, TAC3, TACR3, TAF4B, TEX11, WNT4, WT1, WWOX , (...)
View the complete list with 87 more genes
Specificity
1 %
Genes
100 % |
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ROR2, SALL1, BMP15, BMP4, SEMA3A, SEMA3E, BMP7, FOXL2, BRDT, SOS1, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, AURKC , (...)
View the complete list with 187 more genes
Specificity
1 %
Genes
100 % |
PLCZ1.
By Fulgent Genetics Fulgent Genetics (United States).
PLCZ1
Specificity
100 %
Genes
100 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA; NSLL JOUBERT SYNDROME 16; JBTS16 PSEUDOXANTHOMATOUS DIFFUSE CUTANEOUS MASTOCYTOSIS KERATOSIS, SEBORRHEIC BENIGN FAMILIAL NEONATAL EPILEPSY MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ