WNT3A gene related symptoms and diseases
All the information presented here about the WNT3A gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,ORPHANET,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to WNT3A gene
Symptoms // Phenotype | % Cases |
---|---|
Pain | Very Common - Between 80% and 100% cases |
Gait disturbance | Very Common - Between 80% and 100% cases |
Kyphosis | Very Common - Between 80% and 100% cases |
Osteoporosis | Very Common - Between 80% and 100% cases |
Recurrent fractures | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with WNT3A gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Bone pain
- Hypercalciuria
- Pathologic fracture
- Hyperparathyroidism
- Vertebral compression fractures
- Secondary hyperparathyroidism
- Low serum calcitriol
Rare diseases associated to WNT3A gene
Here you will find a list of rare diseases related to the WNT3A. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
IDIOPATHIC JUVENILE OSTEOPOROSIS
Alternate names
IDIOPATHIC JUVENILE OSTEOPOROSIS Is also known as idiopathic juvenile osteoporosis, juvenile osteoporosis, ijo
Description
Idiopathic juvenile osteoporosis (IJO) is a primary condition of bone demineralization that presents with pain in the back and extremities, walking difficulties, multiple fractures, and radiological evidence of osteoporosis.
Most common symptoms of IDIOPATHIC JUVENILE OSTEOPOROSIS
- Pain
- Gait disturbance
- Kyphosis
- Osteoporosis
- Recurrent fractures
More info about IDIOPATHIC JUVENILE OSTEOPOROSIS
Search interest in WNT3A
Potential gene panels for WNT3A gene
WNT3A Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the WNT3A gene.
More info about this panelTempus xO assay Panel
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 panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HECW2 BUB1B ABCC8 POC1A ARHGEF18 MBD5 ANKRD26