PRMT7 gene related symptoms and diseases
All the information presented here about the PRMT7 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to PRMT7 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Very Common - Between 80% and 100% cases |
| Broad nasal tip | Very Common - Between 80% and 100% cases |
| Obesity | Very Common - Between 80% and 100% cases |
| Retrognathia | Very Common - Between 80% and 100% cases |
| Deeply set eye | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with PRMT7 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Severe global developmental delay
- Astigmatism
- Thin vermilion border
- Short foot
- Delayed myelination
- Long philtrum
- Short metacarpal
- Short palpebral fissure
And 28 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to PRMT7 gene
Here you will find a list of rare diseases related to the PRMT7. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SHORT STATURE-BRACHYDACTYLY-OBESITY-GLOBAL DEVELOPMENTAL DELAY SYNDROME
Alternate names
SHORT STATURE-BRACHYDACTYLY-OBESITY-GLOBAL DEVELOPMENTAL DELAY SYNDROME Is also known as sbidds
Most common symptoms of SHORT STATURE-BRACHYDACTYLY-OBESITY-GLOBAL DEVELOPMENTAL DELAY SYNDROME
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Generalized hypotonia
More info about SHORT STATURE-BRACHYDACTYLY-OBESITY-GLOBAL DEVELOPMENTAL DELAY SYNDROME
Search interest in PRMT7
Potential gene panels for PRMT7 gene
Monogenic Obesity Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Monogenic Obesity Sequencing Panel that also includes the following genes: SDCCAG8 SIM1 UCP3 ARL6 TRIM32 AFF4 PHF6 SETD2 BBS7 TTC8
More info about this panel United States.
Monogenic Obesity Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Monogenic Obesity Deletion/Duplication Panel that also includes the following genes: SDCCAG8 SIM1 UCP3 ARL6 TRIM32 AFF4 PHF6 SETD2 BBS7 TTC8
More info about this panel United States.
Mental retardation - different panels Panel
Germany.
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 panel Germany.
PRMT7 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the PRMT7 gene.
More info about this panel United States.
Tempus xO assay Panel
United States.
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
More info about this panel United States.
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