2008-05-26T00:19:38+00:00
<p>Baller Gerold Syndrome is a rare disorder characterized by abnormalities of certain skull bones and of bones in the arms and hands.</p>
<p>Baller Gerold Syndrome is a rare disorder characterized by abnormalities of certain skull bones and of bones in the arms and hands.</p>
1089
Baller Gerold Syndrome
1
baller-gerold-syndrome
0
Per 100,000 Population
Baller-Gerold syndrome
0
0
2009-09-29T15:23:42+00:00
2009-08-19T20:56:44+00:00
<p>Bangstad syndrome is an inherited congenital disorder associated with abnormalities of the cell membrane.</p>
<p>Bangstad syndrome is an inherited congenital disorder associated with abnormalities of the cell membrane.</p>
1415
Bangstad Syndrome
0
bangstad-syndrome
0
Per 100,000 Population
0
0
2009-08-19T21:03:08+00:00
2009-09-20T15:37:12+00:00
<p>Bannayan-Riley-Ruvalcaba syndrome (<span class="caps">BRRS</span>) is a rare hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.</p>
<p>Bannayan-Riley-Ruvalcaba syndrome (<span class="caps">BRRS</span>) is a rare hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.</p>
1438
Bannayan Riley Ruvalcaba Syndrome
1
bannayan-riley-ruvalcaba-syndrome
0
Per 100,000 Population
Bannayan-Riley-Ruvalcaba Syndrome, BRRS
0
0
2009-09-20T15:37:12+00:00
2009-08-19T20:58:14+00:00
<p>Banti’s Syndrome is a chronic congestive enlargement of the spleen.</p>
<p>Banti’s Syndrome is a chronic congestive enlargement of the spleen.</p>
1416
Banti's Syndrome
0
banti-s-syndrome
0
Per 100,000 Population
Bantis Syndrome, Banti's Disease, Bantis Disease
0
0
2009-08-19T21:04:30+00:00
2008-05-21T13:25:34+00:00
<p>Bardet-Biedl Syndrome is a ciliopathic human genetic disorder that produces many effects and affects many body systems.</p>
<p>Bardet-Biedl Syndrome is a ciliopathic human genetic disorder that produces many effects and affects many body systems.</p>
892
Bardet-Biedl Syndrome
0
bardet-biedl-syndrome
0
0.8
http://www.orpha.net
Per 100,000 Population
Laurence-Moon-Biedl Syndrome, Laurence-Moon-Biedl-Bardet Syndrome, Bardet Biedl Syndrome
0
0
2009-08-19T21:05:38+00:00
2009-08-19T21:02:52+00:00
<p>Bare Lymphocyte Syndrome is a form of severe combined immunodeficiency caused by deficiencies in major histocompatibility.</p>
<p>Bare Lymphocyte Syndrome is a form of severe combined immunodeficiency caused by deficiencies in major histocompatibility.</p>
1417
Bare Lymphocyte Syndrome
0
bare-lymphocyte-syndrome
0
Per 100,000 Population
0
0
2009-08-19T21:07:48+00:00
2008-05-23T20:00:11+00:00
<p>Barre-Lieou Syndrome is a rare disorder characterized by trauma or arthritic changes involving the third and fourth cervical vertebrae or cervical disk lesions with provocation of the cranial nuclei.</p>
<p>Barre-Lieou Syndrome is a rare disorder characterized by trauma or arthritic changes involving the third and fourth cervical vertebrae or cervical disk lesions with provocation of the cranial nuclei.</p>
1055
Barre-Lieou Syndrome
1
barre-lieou-syndrome
0
Per 100,000 Population
Cervicocranial Syndrome, Posterior Cervical Sympathetic Syndrome, Barré-Lieou syndrome, Barre Lieou syndrome
0
0
2009-08-05T13:21:58+00:00
2009-02-20T23:05:11+00:00
<p>Barrett’s Esophagus is an abnormal change in the cells of the esophagus caused by stomach acid.</p>
<p>Barrett’s Esophagus is an abnormal change in the cells of the esophagus caused by stomach acid.</p>
1358
Barrett's Esophagus
2
barrett-s-esophagus
0
Per 100,000 Population
Barrett's syndrome, CELLO, columnar epithelium lined lower oesophagus, Barretts Esophagus
0
1
2010-03-02T07:19:42+00:00
2008-05-21T13:25:35+00:00
<p>Bartter Syndrome is a rare genetic disordercharacterized by low potassium levels and decreased acidity of blood.</p>
<p>Bartter Syndrome is a rare genetic disordercharacterized by low potassium levels and decreased acidity of blood.</p>
1000
Bartter Syndrome
0
bartter-syndrome
0
0.12
http://www.orpha.net
Per 100,000 Population
Bartter's Syndrome, Bartter Syndrome, neonatal Bartter syndrome, classic Bartter syndrome
0
0
2009-08-19T21:13:08+00:00
2008-05-21T13:25:33+00:00
<p>Batten disease is a rare autosomal recessive neurodegenerative disorder beginning in childhood.</p>
<p>Batten disease is a rare autosomal recessive neurodegenerative disorder beginning in childhood.</p>
735
Batten Disease
0
batten-disease
0
4.0
http://www.orpha.net
Per 100,000 Population
Spielmeyer-Vogt-Sjögren-Batten Disease, Subset of Lysosomal Storage Disease and Neuronal Ceroid Lipofuscinosis
0
0
2010-02-09T23:09:48+00:00
2009-07-21T12:47:38+00:00
<p>Bazex–Dupré–Christol Syndrome is a disease of the hair follicle, exhibiting milia, and basal cell cancer during the second decade.</p>
<p>Bazex–Dupré–Christol Syndrome is a disease of the hair follicle, exhibiting milia, and basal cell cancer during the second decade.</p>
1404
Bazex–Dupré–Christol Syndrome
1
bazex–dupre–christol-syndrome
0
Per 100,000 Population
BDC, Bazex Dupré Christol Syndrome, Bazex–Dupré Syndrome, Bazex Dupré Syndrome
0
0
2009-07-21T12:47:38+00:00
2008-08-21T20:14:41+00:00
<p>Beals-Hecht Syndrome is a genetic disorder similar to Marfan’s Syndrome that affects connective tissue.</p>
<p>Beals-Hecht Syndrome is a genetic disorder similar to Marfan’s Syndrome that affects connective tissue.</p>
1200
Beals-Hecht Syndrome
3
beals-hecht-syndrome
0
Per 100,000 Population
Beals syndrome, Congenital contractural arachnodactyly, CCA, BHS, Beals Hecht Syndrome
0
3
2010-02-05T21:05:40+00:00
2008-05-21T13:25:33+00:00
<p>Beckwith-Wiedemann Syndrome is a congenial disorder characterized by an increased risk of childhood cancer and certain features including a large tongue, abdominal wall defects and low blood sugar.</p>
<p>Beckwith-Wiedemann Syndrome is a congenial disorder characterized by an increased risk of childhood cancer and certain features including a large tongue, abdominal wall defects and low blood sugar.</p>
663
Beckwith-Wiedemann Syndrome
1
beckwith-wiedemann-syndrome
0
7.3
http://www.orpha.net
Per 100,000 Population
BWS, Beckwith Wiedemann
0
0
2009-08-05T13:23:54+00:00
<p>The primary cause of Behcet’s Disease is unknown. It is more prevalent in the Middle East and Asia, which suggests a cause endemic to the tropical areas.</p>
2008-05-21T13:25:34+00:00
<p>Behcet’s Disease is a rare disorder characterized by chronic inflammation in blood vessels throughout the body.</p>
<p>Behcet’s Disease is a rare disorder characterized by chronic inflammation in blood vessels throughout the body. The body’s immune system becomes overactive and produces unpredictable outbreaks of exaggerated inflammation. The inflammation, and can be anywhere where there is a blood supply.</p>
<p>There are several symptoms that affect people with Behcet’s Disease.</p>
781
Behcet's Disease
7
behcet-s-disease
0
2.5
http://www.orpha.net
Per 100,000 Population
Behcet's Syndrome, Behçet's, Morbus Behçet, Silk Road Disease, Behcets Syndrome, Behcets Disease, Behçet's Disease
0
0
2009-08-05T13:24:53+00:00
2008-11-20T02:32:42+00:00
<p>Behr’s Syndrome is a rare genetic disorder characterized by partial and increasing loss of vision.</p>
<p>Behr’s Syndrome is a rare genetic disorder characterized by partial and increasing loss of vision.</p>
1249
Behr's Syndrome
0
behr-s-syndrome
0
Per 100,000 Population
Behr's Disease, Behr's Optic Atrophy, Behr Syndrome, Behr Disease, Behrs Syndrome, Behrs Disease
0
0
2009-08-05T13:26:06+00:00