Orofacial Cleft 15; Ofc15
Genes related to Orofacial Cleft 15; Ofc15
Clinical FeaturesTop most frequent phenotypes and symptoms related to Orofacial Cleft 15; Ofc15
- Abnormal facial shape
- Low-set ears
- Midface retrusion
- Upslanted palpebral fissure
- Cleft lip
- Protruding ear
And another 14 symptoms. If you need more information about this disease we can help you.
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 researchersCurrently, 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.
Orofacial Cleft 15; Ofc15 Recommended genes panels
|Panel Name, Specifity and genes Tested/covered|
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
You can get up to -7 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.OMIM Genetic Syndrome Finder
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TRIMETHYLAMINURIA; TMAU INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11 LETHAL CONGENITAL CONTRACTURE SYNDROME 2; LCCS2 FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1 STURGE-WEBER SYNDROME; SWS