2009-05-27T13:20:20+00:00
<p>Idiopathic Atrophoderma of Pasini and Pierini is a form of dermal atrophy.</p>
<p>Idiopathic Atrophoderma of Pasini and Pierini is a form of dermal atrophy.</p>
1391
Idiopathic Atrophoderma of Pasini and Pierini
1
idiopathic-atrophoderma-of-pasini-and-pierini
0
Per 100,000 Population
IAPP
0
0
2009-05-27T13:20:20+00:00
2008-12-31T03:39:40+00:00
<p>Idiopathic Autoimmune Hemolytic Anemia is a reduction in the number of red blood cells due to the body’s immune system.</p>
<p>Idiopathic Autoimmune Hemolytic Anemia is a reduction in the number of red blood cells due to the body’s immune system.</p>
1302
Idiopathic Autoimmune Hemolytic Anemia
1
idiopathic-autoimmune-hemolytic-anemia
0
Per 100,000 Population
Idiopathic Autoimmune Hemolytic Anaemia
0
0
2009-02-26T14:46:18+00:00
2008-05-21T13:25:33+00:00
<p>Idiopathic Hypersomnia is a rare sleep disorder characterized by daytime sleepiness.</p>
<p>Idiopathic Hypersomnia is a rare sleep disorder characterized by daytime sleepiness.</p>
740
Idiopathic Hypersomnia
3
idiopathic-hypersomnia
0
4.0
http://www.orpha.net
Per 100,000 Population
0
1
2008-11-23T14:08:29+00:00
2008-05-21T13:25:32+00:00
<p>Idiopathic Pulmonary Fibrosis is a rare pulmonary disorder characterized by scarring of the lungs.</p>
<p>Idiopathic Pulmonary Fibrosis is a rare pulmonary disorder characterized by scarring of the lungs.</p>
2045
554
Idiopathic Pulmonary Fibrosis
6
idiopathic-pulmonary-fibrosis
0
27.0
http://www.orpha.net
Per 100,000 Population
IPF, Cryptogenic Fibrosing Alveolitis
0
1
2009-04-22T17:30:06+00:00
2010-01-04T15:39:55+00:00
<p>Idiopathic Pulmonary Haemosiderosis is a rare lung disorder characterized by alveolar capillary bleeding and accumulation of iron (in the form of haemosiderin) in the lungs.</p>
<p>Idiopathic Pulmonary Haemosiderosis is a rare lung disorder characterized by alveolar capillary bleeding and accumulation of iron (in the form of haemosiderin) in the lungs.</p>
1459
Idiopathic Pulmonary Haemosiderosis
1
idiopathic-pulmonary-haemosiderosis
0
Per 100,000 Population
IPH
0
0
2010-01-04T15:39:55+00:00
2008-12-26T15:50:41+00:00
<p>Idiopathic Sensory Polyneuropathy is a disorder affecting the nerves that has no identifiable primary cause.</p>
<p>Idiopathic Sensory Polyneuropathy is a disorder affecting the nerves that has no identifiable primary cause.</p>
1289
Idiopathic Sensory Polyneuropathy
1
idiopathic-sensory-polyneuropathy
0
Per 100,000 Population
0
0
2008-12-26T15:50:41+00:00
<p>In children, <span class="caps">ITP</span> is often preceded by a virus. In adults, cause is unknown.</p>
2008-05-23T23:41:13+00:00
<p>Idiopathic Thrombocytopenic Purpura is a condition in which the blood does not clot as quickly as it should due to a low number of platelets.</p>
<p>Diagnosis is one of exclusion. When platelet counts are less than 100,000, other causes of low platelets are examined, and if none exist, then the diagnosis is Idiopathic (or immune) Thrombocytopenic Purpura.</p>
<p>Idiopathic Thrombocytopenic Purpura is a condition in which the blood does not clot as quickly as it should due to a low number of platelets. This may result in bleeding problems.</p>
<p>Bruising, prolonged bleeding and nosebleeds.</p>
<p>Many patients complain of fatigue when counts are low, to the point where <span class="caps">ITP</span> specialists believe their must be a connection to <span class="caps">ITP</span>, but there is no explanation for that connection.</p>
<p><span class="caps">CBC</span></p>
<p>Bone Marrow Biopsy (in older patients or patients considering splenectomy as a treatment option)</p>
<p>Corticosteroids<br />
Anti-D<br />
Anti CD20 (Rituximab)<br />
Splenectomy</p>
<p>In clinical trials at the moment and close to availability: <span class="caps">TPO</span> Agonists that increase platelet production.</p>
1059
Idiopathic Thrombocytopenic Purpura
10
idiopathic-thrombocytopenic-purpura
0
Per 100,000 Population
<p>80% of Children have “acute” cases which resolve within 6-12 months.</p>
<p>20% of Adults seem to have “acute” cases, 80% are considered chronic, but many of those do not require treatment.</p>
Immune Thrombocytopenic Purpura, ITP, Autoimmune Thrombocytopenic Purpura, ATP, TTP, Moschcowitz disease, Idiopathic thrombotic thrombocytopenic purpura, Idiopathic TTP, thrombotic thrombocytopenic purpura
0
1
2009-02-11T13:46:37+00:00
2008-12-25T05:46:06+00:00
<p>IgA Nephropathy is a kidney disease that occurs when the antibody IgA lodges in your kidneys.</p>
<p>IgA Nephropathy is a kidney disease that occurs when the antibody IgA lodges in your kidneys.</p>
1285
IgA Nephropathy
3
iga-nephropathy
0
Per 100,000 Population
Berger's Disease, Berger Disease, IgAN
0
0
2008-12-25T05:46:06+00:00
2008-05-21T13:25:33+00:00
674
Iminoglycinuria
0
iminoglycinuria
0
6.68
http://www.orpha.net
Per 100,000 Population
familial iminoglycinuria
0
0
2009-07-02T18:35:27+00:00
2008-05-21T13:25:34+00:00
<p>Inclusion Body Myositis is a rare inflammatory muscle disease.</p>
<p>Inclusion Body Myositis is a rare inflammatory muscle disease.</p>
<p>Muscle Weakness</p>
927
Inclusion Body Myositis
3
inclusion-body-myositis
0
0.49
http://www.orpha.net
Per 100,000 Population
IBM, Sporadic Inclusion Body Myositis, sIBM,
0
0
2008-08-27T19:48:29+00:00
2008-05-21T13:25:35+00:00
<p>Incontinentia Pigmenti is a genetic disorder that affects the skin, hair, teeth, and nails.</p>
<p>Incontinentia Pigmenti is a genetic disorder that affects the skin, hair, teeth, and nails.</p>
980
Incontinentia Pigmenti
1
incontinentia-pigmenti
0
0.2
http://www.orpha.net
Per 100,000 Population
Bloch-Sulzberger disease, Bloch Siemens syndrome, melanoblastosis cutis, naevus pigmentosus systematicus
0
0
2009-12-11T14:15:46+00:00
2008-07-04T05:34:26+00:00
<p>Intestinal Pseudo Obstruction is a rare disorder characterized by the decreased ability of the intestines to push food through.</p>
<p>Intestinal Pseudo Obstruction is a rare disorder characterized by the decreased ability of the intestines to push food through.</p>
1125
Intestinal Pseudo Obstruction
0
intestinal-pseudo-obstruction
0
Per 100,000 Population
Intestinal pseudoobstruction, Ogilvie syndrome
0
0
2008-07-04T05:35:41+00:00
2008-12-26T15:03:50+00:00
<p>Intracranial Lipomas are rare congenital malformations, usually pericallosal asymptomatic midline lesions.</p>
<p>Intracranial Lipomas are rare congenital malformations, usually pericallosal asymptomatic midline lesions.</p>
1286
Intracranial Lipoma
1
intracranial-lipoma
0
Per 100,000 Population
0
0
2008-12-26T15:05:13+00:00
2008-07-05T16:20:12+00:00
<p>Iritis is characterized by the inflammation of the iris of the eye.</p>
<p>Iritis is characterized by the inflammation of the iris of the eye. There are two types of iritis, acute and chronic.</p>
1129
Iritis
4
iritis
0
Per 100,000 Population
0
0
2008-07-05T16:20:12+00:00
2008-09-22T01:39:39+00:00
<p>Isaac’s Syndrome is a rare neuromuscular disorder.</p>
<p>Isaac’s Syndrome is a rare neuromuscular disorder.</p>
<p>There are several symptoms that affect patients with Isaac’s Syndrome.</p>
<p>There is no cure for Isaac’s Syndrome.</p>
1207
Isaac's Syndrome
3
isaac-s-syndrome
0
Per 100,000 Population
Neuromyotonia, Isaac-Mertens Syndrome, Continuous Muscle Fiber Activity Syndrome, Quantal Squander Syndrome, Isaacs Syndrome
0
0
2009-11-03T19:07:47+00:00