Meier-gorlin Syndrome 5; Mgors5
Clinical Features
Top most frequent phenotypes and symptoms related to Meier-gorlin Syndrome 5; Mgors5
- Microcephaly
- Failure to thrive
- Micrognathia
- Cleft palate
- Cryptorchidism
- Low-set ears
- Feeding difficulties
- Motor delay
- Intrauterine growth retardation
- Long philtrum
And another 20 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.)— The onset for some of the known clinical features related to this disease may vary, including infantile onset, and infantile 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.Meier-gorlin Syndrome 5; Mgors5 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Genetic Services Laboratory University of Chicago (United States).
ORC6, CDC6, GMNN, CDT1, ORC1, ORC4
Specificity
17 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
PLK4, XRCC4, CRIPT, PCNT, ORC6, CENPJ, CDC6, GMNN, RTTN, CDK5RAP2, CUL7, POC1A, CDT1, LARP7, CCDC8, SASS6, CEP63, OBSL1, CEP152, DNA2 , (...)
View the complete list with 8 more genes
Specificity
4 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
STIL, SLC2A1, SLC9A6, PLK4, CDKL5, TCF4, UBE3A, WWOX, RAB18, CRIPT, SLC25A19, ZEB2, CASK, TSEN34, ZNF335, ARFGEF2, PCNT, TBC1D20, TUBGCP4, STAMBP , (...)
View the complete list with 50 more genes
Specificity
2 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
STIL, SLC1A4, SLC2A1, SLC9A6, SOX11, PLK4, CDKL5, TCF4, UBE3A, USP18, WWOX, RAB18, CRIPT, SLC25A19, ZEB2, NIN, PPP1R15B, CASK, TSEN34, ZNF335 , (...)
View the complete list with 59 more genes
Specificity
2 %
Genes
100 % |
![]() By Molecular Diagnostics Lab Nemours Alfred I. duPont Hospital for Children (United States).
CDC6
Specificity
100 %
Genes
100 % |
![]() By PreventionGenetics PreventionGenetics (United States).
ORC6, CDC6, CDT1, ORC1, ORC4
Specificity
20 %
Genes
100 % |
![]() By PreventionGenetics PreventionGenetics (United States).
CDC6
Specificity
100 %
Genes
100 % |
![]() By PreventionGenetics PreventionGenetics (United States).
RMRP, ROR2, RUNX2, SALL1, BMP1, BMP2, BMPR1B, SF3B4, SH3BP2, FBXW4, SHH, SHOX, SKI, SLCO2A1, SLC26A2, SMARCAL1, SMC1A, SOX9, SQSTM1, TBX15 , (...)
View the complete list with 236 more genes
Specificity
1 %
Genes
100 % |
You can get up to 22 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 RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS; RAMSVPS PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR COFFIN-SIRIS SYNDROME 4; CSS4 ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 FATAL FAMILIAL INSOMNIA; FFI OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; OSMEDB HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES; HGCLAS