2008-11-21T15:29:26+00:00
<p>X Chromosome Duplication is the duplication of chromosome X between Xq27.2 and Xq28.</p>
<p>X Chromosome Duplication is the duplication of chromosome X between Xq27.2 and Xq28.</p>
1253
X Chromosome Duplication
1
x-chromosome-duplication
0
Per 100,000 Population
X Chromosome duplication between Xq27.2 and Xq28
0
0
2010-02-12T18:47:07+00:00
2008-05-21T13:25:34+00:00
<p>X-Linked Agammaglobulinemia is a rare X-linked genetic disorder that affects the body’s ability to fight infection.</p>
<p>X-Linked Agammaglobulinemia is a rare X-linked genetic disorder that affects the body’s ability to fight infection.</p>
928
X-Linked Agammaglobulinemia
1
x-linked-agammaglobulinemia
0
0.45
http://www.orpha.net
Per 100,000 Population
X-Linked Hypogammaglobulinemia, XLA, Bruton Type Agammaglobulinemia, X Linked Agammaglobulinemia
0
0
2009-08-07T04:03:33+00:00
2010-03-05T14:24:26+00:00
<p>X-linked Alpha Thalassemia Mental Retardation Syndrome is a rare inherited disorder affecting multiple body functions including intellectual development and muscle development.</p>
<p>X-linked Alpha Thalassemia Mental Retardation Syndrome is a rare inherited disorder affecting multiple body functions including intellectual development and muscle development.</p>
1472
X-linked Alpha Thalassemia Mental Retardation Syndrome
1
x-linked-alpha-thalassemia-mental-retardation-syndrome
0
Per 100,000 Population
Alpha thalassemia X-linked mental retardation syndrome, ATRX Syndrome
0
0
2010-03-05T14:24:26+00:00
2008-05-21T13:25:34+00:00
<p>X-linked Dominant Chondrodysplasia Punctata is a rare genetic disorder affecting skeletal development and characterized by abnormal accumulations of calcium salts within the growing ends of long bones.</p>
<p>X-linked Dominant Chondrodysplasia Punctata is a rare genetic disorder affecting skeletal development and characterized by abnormal accumulations of calcium salts within the growing ends of long bones.</p>
926
X-linked Dominant Chondrodysplasia Punctata
0
x-linked-dominant-chondrodysplasia-punctata
0
0.5
http://www.orpha.net
Per 100,000 Population
X linked dominant chondrodysplasia punctata, Conradi-Hünermann syndrome, Conradi Hünermann syndrome, Conradi–Hünermann–Happle syndrome, Conradi Hünermann Happle syndrome
0
0
2010-02-05T16:55:38+00:00
2009-12-14T13:54:36+00:00
<p>X-linked Hypophosphatemia is an rare genetic form of rickets in which the ingestion of Vitamin D is relatively ineffective.</p>
<p>X-linked Hypophosphatemia is an rare genetic form of rickets in which the ingestion of Vitamin D is relatively ineffective.</p>
1457
X-linked Hypophosphatemia
0
x-linked-hypophosphatemia
0
Per 100,000 Population
hypophosphatemic rickets, vitamin D-resistant rickets
0
0
2009-12-14T13:54:36+00:00
2008-05-21T13:25:32+00:00
<p>X-Linked Ichthyosis is a rare skin disorder caused by the hereditary deficiency of the steroid sulfatase (<span class="caps">STS</span>) enzyme.</p>
<p>X-Linked Ichthyosis is a rare skin disorder caused by the hereditary deficiency of the steroid sulfatase (<span class="caps">STS</span>) enzyme.</p>
583
X-Linked Ichthyosis
3
x-linked-ichthyosis
0
16.6
http://www.orpha.net
Per 100,000 Population
XLI, X Linked Ichthyosis
0
0
2009-08-07T04:05:28+00:00
2008-05-21T13:25:35+00:00
<p>X-Linked Lymphoproliferative Disease is a rare immunodeficiency disorder characterized by an underactive or overactive immune system.</p>
<p>X-Linked Lymphoproliferative Disease is a rare immunodeficiency disorder characterized by an underactive or overactive immune system.</p>
1021
X-Linked Lymphoproliferative Disease
6
x-linked-lymphoproliferative-disease
0
0.1
http://www.orpha.net
Per 100,000 Population
Duncan's Syndrome, Duncans Syndrome, XLP, X-Linked Lymphoproliferative Syndrome, X Linked Lymphoproliferative Disease
0
0
2009-08-07T04:06:31+00:00
2008-05-21T13:25:34+00:00
<p>X-linked Ocular Albinism is a rare form of albinism that presents primarily in the eyes.</p>
<p>X-linked Ocular Albinism is a rare form of albinism that presents primarily in the eyes.</p>
810
X-linked Ocular Albinism
0
x-linked-ocular-albinism
0
2.0
http://www.orpha.net
Per 100,000 Population
X-linked Recessive Ocular Albinism, XLOA, X linked Ocular Albinism
0
0
2009-08-07T04:07:34+00:00
2008-05-21T13:25:34+00:00
<p>Xeroderma pigmentosum is an autosomal recessive genetic disorder of <span class="caps">DNA</span> repair in which the ability to repair damage caused by ultraviolet (UV) light is deficient.</p>
<p>Xeroderma pigmentosum is an autosomal recessive genetic disorder of <span class="caps">DNA</span> repair in which the ability to repair damage caused by ultraviolet (UV) light is deficient.</p>
925
Xeroderma pigmentosum
0
xeroderma-pigmentosum
0
0.5
http://www.orpha.net
Per 100,000 Population
XP
0
0
2008-06-28T23:37:20+00:00
2008-05-21T13:25:32+00:00
<p>XX Gonadal Dysgenesis is a disorder of the female reproductive system in which functional ovaries are not present to induce puberty.</p>
<p>XX Gonadal Dysgenesis is a disorder of the female reproductive system in which functional ovaries are not present to induce puberty.</p>
612
XX Gonadal Dysgenesis
1
xx-gonadal-dysgenesis
0
12.0
http://www.orpha.net
Per 100,000 Population
0
1
2009-12-02T03:20:26+00:00