Diaphragmatic Hernia 3; Dih3
Clinical Features
Phenotypes and symptoms related to Diaphragmatic Hernia 3; Dih3
- Ventricular septal defect
- Hernia
- Congenital diaphragmatic hernia
- Overriding aorta
- Posterolateral diaphragmatic hernia
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.Diaphragmatic Hernia 3; Dih3 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
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Abnormal/Ambiguous Genitalia Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
ROR2, SALL1, BMP4, SEMA3A, SOX9, SRD5A2, SRY, STAR, TBX15, CEP41, TSPYL1, WNT4, WNT7A, WT1, SETBP1, ZFPM2, UBR1, FIG4, IL17RD, CDKN1C , (...)
View the complete list with 52 more genes
Specificity
2 %
Genes
50 % |
46,XY Disorders of Sex Development/Complete Gonadal Dysgenesis Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
SOX9, SRD5A2, SRY, WT1, ZFPM2, ARX, B3GLCT, MAMLD1, CYB5A, CYP11A1, CYP17A1, DHCR7, DHH, DYNC2H1, AKR1C2, GATA4, AMH, AMHR2, HCCS, HSD17B3 , (...)
View the complete list with 6 more genes
Specificity
4 %
Genes
50 % |
46,XY Disorders of Sex Development/Complete Gonadal Dysgenesis Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
SOX9, SRD5A2, SRY, WT1, ZFPM2, ARX, B3GLCT, MAMLD1, CYB5A, CYP11A1, CYP17A1, DHCR7, DHH, DYNC2H1, AKR1C2, GATA4, AMH, AMHR2, HCCS, HSD17B3 , (...)
View the complete list with 6 more genes
Specificity
4 %
Genes
50 % |
Hypospadias Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SALL1, BMP4, BMP7, SOX2, SRD5A2, HNF1B, MED12, WNT7A, WT1, FBXL4, WDR11, ZEB2, SETBP1, TP63, PCNT, ZFPM2, UBR1, FIG4, CDKN1C, ARX , (...)
View the complete list with 53 more genes
Specificity
2 %
Genes
50 % |
Isolated Nonsyndromic Congenital Heart Defects via ZFPM2 (FOG2) Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ZFPM2
Specificity
100 %
Genes
50 % |
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
50 % |
Disorders of Sex Development (DSD) Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ROR2, SALL1, BMP15, BMP4, SEMA3A, BMP7, FOXL2, SOS1, SOX10, SOX2, SOX3, SOX9, SRD5A2, SRY, STAR, TAC3, TACR3, TBX15, HNF1B, MED12 , (...)
View the complete list with 138 more genes
Specificity
1 %
Genes
50 % |
Ambiguous Genitalia Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ROR2, SALL1, BMP4, SEMA3A, SOS1, SOX10, SOX2, SOX3, SOX9, SRD5A2, SRY, STAR, TBX15, CEP41, TSPYL1, WNT4, WNT5A, WNT7A, WT1, WWOX , (...)
View the complete list with 65 more genes
Specificity
2 %
Genes
50 % |
You can get up to 14 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
MESH OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT BARDET-BIEDL SYNDROME 7; BBS7 CHROMOSOME 17q11.2 DELETION SYNDROME, 1.4-MB ENCHONDROMATOSIS LIDDLE SYNDROME; LIDLS MCCUNE-ALBRIGHT SYNDROME; MAS EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48; EIEE48