Orofacial Cleft 5; Ofc5
Clinical Features
Phenotypes and symptoms related to Orofacial Cleft 5; Ofc5
- Cleft palate
- Cleft upper lip
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
Orofacial Cleft 5; Ofc5 Is also known as cleft lip with or without cleft palate, nonsyndromic, 5.
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.
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Orofacial Cleft 5; Ofc5 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Orofacial cleft 5 (sequence analysis of MSX1 gene).
By CGC Genetics (Portugal).
MSX1
Specificity
100 %
Genes
100 % |
|
Ectodermal dysplasia (NGS panel for 8 genes).
By CGC Genetics (Portugal).
EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1
Specificity
13 %
Genes
100 % |
|
Ectodermal dysplasia (NGS panel for 8 genes).
By CGC Genetics (Portugal).
EDARADD, KRT74, EDAR, EDA, GJB6, HOXC13, KRT85, MSX1
Specificity
13 %
Genes
100 % |
 Ectodermal Dysplasia/Tooth Agenesis via MSX1 Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
MSX1
Specificity
100 %
Genes
100 % |
|
Tooth Agenesis Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
WNT10A, EDARADD, EDAR, EDA, LTBP3, MSX1, PAX9, AXIN2
Specificity
13 %
Genes
100 % |
|
Cleft lip, cleft palate and related disorders NGS panel.
By Connective Tissue Gene Tests (United States).
BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1
Specificity
7 %
Genes
100 % |
|
Cleft lip, cleft palate and related disorders Deletion / Duplication panel.
By Connective Tissue Gene Tests (United States).
BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1
Specificity
7 %
Genes
100 % |
|
Cleft lip, cleft palate and related disorders Comprehensive panel.
By Connective Tissue Gene Tests (United States).
BMP4, TBX22, SUMO1, TP63, TGDS, SATB2, COL11A1, COL11A2, COL9A1, COL9A2, COL9A3, GRHL3, FOXE1, IRF6, MSX1, NECTIN1
Specificity
7 %
Genes
100 % |
Sources and references
You can check the following sources for additional information.
OMIM MESH Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION; CFTD MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D EHLERS-DANLOS SYNDROME WITH SHORT STATURE AND LIMB ANOMALIES; EDSSLA PITT-HOPKINS SYNDROME; PTHS BEHAVIORAL VARIANT OF FRONTOTEMPORAL DEMENTIA COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1 ABSENCE OF FINGERPRINTS-CONGENITAL MILIA SYNDROME
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