MEIS2 gene related symptoms and diseases
All the information presented here about the MEIS2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to MEIS2 gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Very Common - Between 80% and 100% cases |
Atrial septal defect | Very Common - Between 80% and 100% cases |
Narrow forehead | Very Common - Between 80% and 100% cases |
Abnormal cardiac septum morphology | Very Common - Between 80% and 100% cases |
Cleft lip | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with MEIS2 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Deeply set eye
- Tented upper lip vermilion
- Global developmental delay
- Highly arched eyebrow
- Oral cleft
- Ventricular septal defect
- Motor delay
- Low-set ears
And 58 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to MEIS2 gene
Here you will find a list of rare diseases related to the MEIS2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR
Alternate names
CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR Is also known as cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
Most common symptoms of CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR
- Intellectual disability
- Global developmental delay
- Short stature
- Microcephaly
- Abnormal facial shape
More info about CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR
15Q14 MICRODELETION SYNDROME
Alternate names
15Q14 MICRODELETION SYNDROME Is also known as del(15)(q14), monosomy 15q14
Description
15q14 microdeletion syndrome is a recently described syndrome characterized by developmental delay, short stature and facial dysmorphism.
Most common symptoms of 15Q14 MICRODELETION SYNDROME
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Generalized hypotonia
More info about 15Q14 MICRODELETION SYNDROME
Search interest in MEIS2
Potential gene panels for MEIS2 gene
Mental retardation - different panels Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Mental retardation - different panels that also includes the following genes: RGS7 RIT1 RMRP BCS1L RPL10 RPS6KA3 RRAS SALL1 SC5D ATXN10
More info about this panelInvitae Congenital Heart Defects and Heterotaxy Panel Panel
By Invitae Invitae Congenital Heart Defects and Heterotaxy Panel that also includes the following genes: RIT1 RPGR BRAF SOS1 SPAG1 TBX1 TBX5 RSPH1 ZIC3 CFAP298
More info about this panelInvitae Congenital Heart Disease Panel Panel
By Invitae Invitae Congenital Heart Disease Panel that also includes the following genes: RIT1 BRAF SOS1 TBX1 TBX5 ZIC3 NSD1 ACTC1 CRELD1 CBL
More info about this panelMEIS2 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the MEIS2 gene.
More info about this panelCongenital Structural Heart Disease Panel Panel
By Blueprint Genetics Congenital Structural Heart Disease Panel that also includes the following genes: BMPR2 SOS2 TBX1 TBX20 TBX5 TFAP2B TLL1 ZIC3 ACTA2 ACTB
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like KCND2 GCKR VARS2 KARS EBF3 GATA2 ADAR