NUP98 gene related symptoms and diseases
All the information presented here about the NUP98 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NUP98 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Very Common - Between 80% and 100% cases |
| Long nose | Very Common - Between 80% and 100% cases |
| Sloping forehead | Very Common - Between 80% and 100% cases |
| Aganglionic megacolon | Very Common - Between 80% and 100% cases |
| Long eyelashes | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NUP98 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Low anterior hairline
- Increased body weight
- Abnormal autonomic nervous system physiology
- Adducted thumb
- Failure to thrive in infancy
- Intestinal obstruction
- Flat occiput
- Malnutrition
And 42 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NUP98 gene
Here you will find a list of rare diseases related to the NUP98. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
HIRSCHSPRUNG DISEASE
Alternate names
HIRSCHSPRUNG DISEASE Is also known as hscr, aganglionic megacolon, congenital intestinal aganglionosis, hirschsprung disease, megacolon, aganglionic, mgc
Description
Hirschsprung disease (HSCR) is a congenital intestinal motility disorder that is characterized by signs of intestinal obstruction due to the presence of an aganglionic segment of variable extent in the terminal part of the colon.
Most common symptoms of HIRSCHSPRUNG DISEASE
- Intellectual disability
- Global developmental delay
- Short stature
- Hearing impairment
- Microcephaly
More info about HIRSCHSPRUNG DISEASE
Search interest in NUP98
Potential gene panels for NUP98 gene
NUP98 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NUP98 gene.
More info about this panel United States.
Onco microarray for MDS/AML Panel
United States.
By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center Onco microarray for MDS/AML that also includes the following genes: BCR RPN1 RUNX1 SET TCF3 TERT TFG TP53 TRPS1 WT1
More info about this panel United States.
FoundationOne® Heme Panel
United States.
By Foundation Medicine, Inc. FoundationOne® Heme that also includes the following genes: BCL6 BCL7A ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1
More info about this panel United States.
Caris MI TumorSeek 592-Gene NGS Panel Panel
United States.
By Caris Life Sciences Caris MI TumorSeek 592-Gene NGS Panel that also includes the following genes: BCL6 BCL7A BCL9 BCR ROS1 RPL10 RPL22 RPL5 RPN1 RUNX1
More info about this panel United States.
Tempus xT assay Panel
United States.
By Tempus Labs, Inc. Tempus xT assay that also includes the following genes: BCL6 RIT1 BCL7A BCR ROS1 RPL5 RPS15 RPS6KB1 RUNX1 RXRA
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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