Orofacial Cleft 10; Ofc10
Clinical Features
Phenotypes and symptoms related to Orofacial Cleft 10; Ofc10
- Cleft lip
- Unilateral cleft lip
- Unilateral cleft palate
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 10; Ofc10 Is also known as cleft lip with or without cleft palate, nonsyndromic, 10.
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 10; Ofc10 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 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 % |
 SUMO1.
By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).
SUMO1
Specificity
100 %
Genes
100 % |
 Orofacial cleft type 10.
By Centogene AG - the Rare Disease Company (Germany).
SUMO1
Specificity
100 %
Genes
100 % |
|
Cleft lip/palate panel.
By Centogene AG - the Rare Disease Company (Germany).
BMP4, SUMO1, TP63, IRF6, MSX1, NECTIN1
Specificity
17 %
Genes
100 % |
 qGenEx Craniofacial Anomalies.
By Quantitative Genomic Medicine Laboratories, SL (Spain).
RUNX2, SALL1, TSHZ1, BMP4, SEMA3E, SF3B4, SH3BP2, SHH, SIX1, SIX3, SKI, SNAI2, SMC1A, SOX10, TBX22, TCF12, TCOF1, TFAP2A, TGFBR1, TGFBR2 , (...)
View the complete list with 114 more genes
Specificity
1 %
Genes
100 % |
|
SUMO1.
By Fulgent Genetics Fulgent Genetics (United States).
SUMO1
Specificity
100 %
Genes
100 % |
Sources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SC PHOCOMELIA SYNDROME GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE GLANZMANN THROMBASTHENIA; GT IMMUNODEFICIENCY 17; IMD17 CORNEAL ENDOTHELIAL DYSTROPHY; CHED GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2 GM2-GANGLIOSIDOSIS, AB VARIANT
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