Search your symptoms with MEDgle. You can check your symptoms. It is a medical symptom search allowing you find out what options make sense for you.
PATIENT GPS
 
english
espanolfrancaisdeutschnederlands中國傳統简体中文日本語
patients healthcare providers how it works about
 
 

symptoms diagnoses drugs procedures physicians
  
 
visual
reduced results from
11B options
600000
80000
3 options
1 - 3 of 3 diseases - gender ? age ?

high nasal bridge

 View    
The results should NOT be considered a diagnosis. Please consult your health care provider.
edit important variables such as: demo: duration, demo: age, lump or swelling in groin in males, heart murmur, life: Family History, cognitive defect, learning problems
related types of physicians - cardiologist, genetics specialist
Shprintzen Syndrome - rare genetic disease with heart defects and abnormal facial features
a.k.a 22q11.2 deletion syndrome, Velocardiofacial Syndrome, DiGeorge Syndrome, conotruncal anomaly face syndrome, Congenital Thymic Aplasia, Strong Syndrome
13q deletion syndrome - rare chromosomal disorder involving long arm of chromosome 13
a.k.a Orbeli syndrome
Opitz Syndrome - rare genetic disease associated with midline abnormalities
a.k.a Smith-Lemli-Opitz syndrome, 7-dehydrocholesterol reductase deficiency

for more please login, login is free (click to login)




faq/about | disclaimer | privacy policy | terms of service | browse | beta | contact | API - Catalyst

MEDgle does not provide medical advice, diagnosis or treatment. Copyright 2006-2012, MEDgle Inc. All Rights Reserved. MEDgle is NOT affiliated with Google. Last Updated: Mar 14, 2012
This website is certified by Health On the Net Foundation. Click to verify. This site complies to the HONcode standard for trustworthy health information: verify here.
 
Invited Sponsor for Communications Conference
 
Finalist -- search & reference
 
MEDgle has been selected for the 2009 Best of Business Award in the Medical research