LMAN2L gene related symptoms and diseases
All the information presented here about the LMAN2L gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to LMAN2L gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Uncommon - Between 30% and 50% cases |
| Seizures | Uncommon - Between 30% and 50% cases |
| Global developmental delay | Uncommon - Between 30% and 50% cases |
| Intellectual disability, severe | Uncommon - Between 30% and 50% cases |
| Poor speech | Uncommon - Between 30% and 50% cases |
Rare diseases associated to LMAN2L gene
Here you will find a list of rare diseases related to the LMAN2L. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52; MRT52
Most common symptoms of MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52; MRT52
- Intellectual disability
- Seizures
- Global developmental delay
- Intellectual disability, severe
- Poor speech
More info about MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52; MRT52
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 LMAN2L
Potential gene panels for LMAN2L gene
LMAN2L Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the LMAN2L gene.
More info about this panel United States.
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