DCPS gene related symptoms and diseases
All the information presented here about the DCPS gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to DCPS gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Uncommon - Between 30% and 50% cases |
| Thin upper lip vermilion | Uncommon - Between 30% and 50% cases |
| Sandal gap | Uncommon - Between 30% and 50% cases |
| Hypopigmentation of the skin | Uncommon - Between 30% and 50% cases |
| Inability to walk | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with DCPS gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Flat face
- Unsteady gait
- Abnormal cardiac septum morphology
- Joint laxity
- Neonatal hypotonia
- Deeply set eye
- Narrow mouth
- Global developmental delay
And 10 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to DCPS gene
Here you will find a list of rare diseases related to the DCPS. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AL-RAQAD SYNDROME; ARS
Most common symptoms of AL-RAQAD SYNDROME; ARS
- Intellectual disability
- Global developmental delay
- Generalized hypotonia
- Microcephaly
- Growth delay
More info about AL-RAQAD SYNDROME; ARS
SOURCES: OMIM
AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY
Alternate names
AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY Is also known as ar-nsid, ns-arid
More info about AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY
SOURCES: ORPHANET
Search interest in DCPS
Potential gene panels for DCPS gene
Non-syndromic Intellectual Disability (NS-ID) Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Non-syndromic Intellectual Disability (NS-ID) Sequencing Panel with CNV Detection that also includes the following genes: BDNF RPS6KA3 SCN2A SCN8A SLC16A2 SLC2A1 SLC6A8 SLC9A6 SMC1A KDM5C
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.
Al-Raqad syndrome Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the DCPS gene.
More info about this panel Germany.
DCPS Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the DCPS gene.
More info about this panel United States.
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