Spermatogenic Failure 13; Spgf13
Clinical Features
Phenotypes and symptoms related to Spermatogenic Failure 13; Spgf13
- Azoospermia
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.
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 13; Spgf13 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
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![]() 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 % |
![]() 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 % |
![]() By Fulgent Genetics Fulgent Genetics (United States).
TAF4B
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 Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2 L-2-HYDROXYGLUTARIC ACIDURIA; L2HGA EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS