2009-05-21T13:23:37+00:00
<p>Sacral Agenesis is a rare spinal deformity affecting the sacrum.</p>
<p>Sacral Agenesis is a rare spinal deformity affecting the sacrum.</p>
1390
Sacral Agenesis
0
sacral-agenesis
0
Per 100,000 Population
Hypoplasia of the Scrum, Cudal Rgression Sndrome
0
0
2009-05-21T13:23:37+00:00
2010-02-14T16:25:46+00:00
<p>Sacrococcygeal Teratoma tumor located at the base of the tailbone.</p>
<p>Sacrococcygeal Teratoma tumor located at the base of the tailbone.</p>
1466
Sacrococcygeal Teratoma
1
sacrococcygeal-teratoma
0
Per 100,000 Population
0
0
2010-02-14T16:25:46+00:00
2008-05-21T13:25:34+00:00
774
Saethre-Chotzen Syndrome
1
saethre-chotzen-syndrome
0
3.0
http://www.orpha.net
Per 100,000 Population
Saethre Chotzen Syndrome, acrocephalosyndactyly type 3, acrocephalosyndactyly type III, ACS III, Chotzen syndrome
0
0
2009-07-27T23:08:21+00:00
2009-02-17T15:54:56+00:00
<p>Salivary Gland Cancer is a rare form of cancer in the salivary glands.</p>
<p>Salivary Gland Cancer is a rare form of cancer in the salivary glands.</p>
1335
Salivary Gland Cancer
0
salivary-gland-cancer
0
Per 100,000 Population
0
0
2009-02-17T15:54:56+00:00
2008-05-21T13:25:34+00:00
<p>Sandhoff Disease is a rare genetic lipid storage disorder.</p>
<p>Sandhoff Disease is a rare genetic lipid storage disorder.</p>
903
Sandhoff Disease
0
sandhoff-disease
0
0.75
http://www.orpha.net
Per 100,000 Population
Jatzkewitz-Pilz Syndrome, Hexosaminidase A and B deficiency, Subset of Lysosomal Storage Disease and GM2 gangliosidoses
0
0
2010-02-09T23:14:33+00:00
2008-05-21T13:25:34+00:00
<p>Sanfilippo Syndrome is a rare autosomal recessive metabolic disorder characterized by severe neurological symptoms.</p>
<p>Sanfilippo Syndrome is a rare autosomal recessive metabolic disorder characterized by severe neurological symptoms.</p>
<p>There are several symptoms that affect people with Mucopolysaccharidosis type 3.</p>
850
Sanfilippo Syndrome
4
sanfilippo-syndrome
0
1.1
http://www.orpha.net
Per 100,000 Population
Mucopolysaccharidosis Type 3, Mucopolysaccharidosis type III, mucopolysaccharide storage disease type III, oligophrenic polydystrophy, polydystrophia oligophrenia, Subset of: Lysosomal Storage Disease and Mucopolysaccharidoses Disorders
0
1
2010-02-09T23:03:12+00:00
2008-07-20T02:17:22+00:00
<p><span class="caps">SAPHO</span> Syndrome is a disorder characterized by synovitis, acne, pustulosis, hyperostosis, and osteitis.</p>
<p><span class="caps">SAPHO</span> Syndrome is a disorder characterized by synovitis, acne, pustulosis, hyperostosis, and osteitis.</p>
<p>There are several symptoms that affect people diagnosed with <span class="caps">SAPHO</span> Syndrome.</p>
<p>Treatment for <span class="caps">SAPHO</span> Syndrome is based on symptoms.</p>
1182
SAPHO Syndrome
4
sapho-syndrome
0
Per 100,000 Population
Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis, Chronic Recurrent Multifocal Osteomyelitis, CRMO
0
0
2008-09-29T04:59:58+00:00
<p>The cause of Sarcoidosis is not known; however, it is thought to be caused by the immune system’s reaction to factors in the environment. Sarcoidosis most commonly affects young adults.</p>
2008-05-21T13:25:32+00:00
<p>Sarcoidosis is a rare immune system disorder characterized by non-caseating granulomas which most often appear in the lungs or the lymph nodes.</p>
<p>Sarcoidosis is a rare immune system disorder characterized by non-caseating granulomas which most often appear in the lungs or the lymph nodes.</p>
<p>There are several symptoms that affect patients with Sarcoidosis.</p>
<p>Thirty to seventy percent of patients do not require therapy.</p>
592
Sarcoidosis
22
sarcoidosis
0
15.0
http://www.orpha.net
Per 100,000 Population
<p>In most cases of Sarcoidosis, the disease spontaneously disappears, requiring no treatment.</p>
Sarcoid, Schaumann's Syndrome, Schaumann Syndrome, Sarcoid, Boeck's Sarcoid, Boeck Sarcoid, Boeck's Disease, Boeck Disease, Besnier-Boeck-Schaumann Syndrome, Besnier-Boeck-Schaumann Disease
0
5
2009-10-06T23:01:21+00:00
2008-05-21T13:25:34+00:00
<p>Sarcosinemia is a rare disorder characterized by increased sarcosine in the blood plasma and urine.</p>
<p>Sarcosinemia is a rare disorder characterized by increased sarcosine in the blood plasma and urine.</p>
813
Sarcosinemia
0
sarcosinemia
0
2.0
http://www.orpha.net
Per 100,000 Population
SAR, Hypersarcosinemia and SARDH deficiency
0
0
2010-02-06T18:04:19+00:00
2008-12-24T23:06:42+00:00
<p>Schamberg Disease is a chronic discoloration of the skin, most commonly affecting the legs.</p>
<p>Schamberg Disease is a chronic discoloration of the skin, most commonly affecting the legs.</p>
1283
Schamberg Disease
1
schamberg-disease
0
Per 100,000 Population
Progressive Pigmented Purpuric Dermatitis, PPPD, Schamberg's Disease
0
0
2008-12-25T05:20:42+00:00
2008-07-05T19:59:54+00:00
<p>Schinzel-Giedion Syndrome is a rare congenital neurodegenerative disorder.</p>
<p>Schinzel-Giedion Syndrome is a rare congenital neurodegenerative disorder.</p>
1145
Schinzel-Giedion Syndrome
1
schinzel-giedion-syndrome
0
30.0
http://ec.europa.eu/health/ph_threats/non_com/docs/rdnumbers.pdf
Cases
SGS, Schinzel-Giedion Midface Retraction Syndrome, Schinzel Giedion Syndrome
0
0
2009-02-07T17:08:16+00:00
2008-05-21T13:25:34+00:00
<p>Schizencephaly is a rare cortical malformation of the brain.</p>
<p>Schizencephaly is a rare cortical malformation of the brain.</p>
827
Schizencephaly
2
schizencephaly
0
1.54
http://www.orpha.net
Per 100,000 Population
Cephalic Disorder
0
0
2009-01-16T16:38:01+00:00
2009-02-19T14:22:03+00:00
<p>Schnitzler Syndrome is a rare disease characterised by chronic hives.</p>
<p>Schnitzler Syndrome is a rare disease characterised by chronic hives.</p>
1351
Schnitzler Syndrome
2
schnitzler-syndrome
0
Per 100,000 Population
Schnitzler's Syndrome, Schnitzlers Syndrome
0
1
2009-12-28T07:03:07+00:00
2008-05-21T13:25:32+00:00
<p>Sclerodrema, also known as systemic sclerosis is a chronic disease in which there are excessive deposits of collagen in various organs.</p>
<p>Diagnosis requires blood tests and other localized test in the specific organs affected.</p>
<p>Since the collagen deposits vary in their locations, symptoms vary widely.</p>
<p>While there is currently no cure for Scleroderma, there are various drugs and treatments that used to treat individual symptoms.</p>
534
Scleroderma
9
scleroderma
0
42.0
http://www.orpha.net
Per 100,000 Population
0
1
2009-12-11T13:56:02+00:00
<p>The cause of Scleromyxedema is unknown, but is most probably autoimmune.</p>
2008-06-18T03:42:39+00:00
<p>Scleromyxedema is a condition of mucinous deposition in the skin associated with monoclonal gammopathy characterized by a flesh-colored, papular skin eruption. The average age onset is 55 years and there was roughly equal distribution of gender.</p>
<p>Scleromyxedema is a condition of mucinous deposition in the skin associated with monoclonal gammopathy characterized by a flesh-colored, papular skin eruption. The average age onset is 55 years and there was roughly equal distribution of gender.</p>
<p>As the disease progresses, mucin deposition progresses to internal organs, joints, and connective tissues thus leading to “stiff man” like scleroderma. As things progress, internal problems can go into the brain and vital organs with bad results.</p>
<p>Deep tissue biopsy and bone marrow biopsy. A skin biopsy is much less invasive.</p>
<p>IVIg</p>
1116
Scleromyxedema
8
scleromyxedema
0
150.0
http://www.mayoclinic.org/
Cases
<p>Current prognosis is poor, but there is more hope with the IVIg treatment.</p>
Lichen Myxedematosus, Papular Mucinosis, Paraproteinemia Associated Desmoplasia
0
1
2009-08-19T16:55:56+00:00