2009-01-09T15:13:27+00:00
<p><span class="caps">LADD</span> Syndrome is a rare genetic disorder characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.</p>
<p><span class="caps">LADD</span> Syndrome is a rare genetic disorder characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.</p>
1309
LADD Syndrome
1
ladd-syndrome
0
Per 100,000 Population
Lacrimo-Auriculo-Dento-Digital Syndrome, Lacrimo Auriculo Dento Digital Syndrome
0
0
2009-01-09T15:13:27+00:00
2008-05-21T13:25:35+00:00
<p>Lafora Disease is a rare genetic disorder characterized by the presence of Lafora bodies, within neurons and the cells of the heart, liver, muscle, and skin.</p>
<p>Lafora Disease is a rare genetic disorder characterized by the presence of Lafora bodies, within neurons and the cells of the heart, liver, muscle, and skin.</p>
1023
Lafora Disease
0
lafora-disease
0
0.1
http://www.orpha.net
Per 100,000 Population
Lafora progressive myoclonic epilepsy
0
0
2010-02-01T22:50:33+00:00
2008-05-21T13:25:34+00:00
<p>Lambert-Eaton Myasthenic Syndrome is a rare autoimmune disorder which affects calcium delivery to the nerve-muscle junctions.</p>
<p>Lambert-Eaton Myasthenic Syndrome is a rare autoimmune disorder which affects calcium delivery to the nerve-muscle junctions.</p>
877
Lambert-Eaton Myasthenic Syndrome
2
lambert-eaton-myasthenic-syndrome
0
1.0
http://www.orpha.net
Per 100,000 Population
LEMS, Lambert Eaton Myasthenic Syndrome
0
0
2009-08-05T03:15:46+00:00
2008-05-21T13:25:35+00:00
<p>Lamellar Ichthyosis is a rare inherited skin disorder.</p>
<p>Lamellar Ichthyosis is a rare inherited skin disorder.</p>
948
Lamellar Ichthyosis
0
lamellar-ichthyosis
0
0.33
http://www.orpha.net
Per 100,000 Population
ichthyosis lammellaris, nonbullous congenital ichthyosis
0
0
2010-01-30T22:48:56+00:00
2008-12-26T16:45:11+00:00
<p>Landau-Kleffner Syndrome is a childhood disorder characterized by the loss of the ability to understand and use spoken language.</p>
<p>Landau-Kleffner Syndrome is a childhood disorder characterized by the loss of the ability to understand and use spoken language.</p>
1292
Landau-Kleffner Syndrome
0
landau-kleffner-syndrome
0
Per 100,000 Population
Landau Kleffner syndrome, LKS, Infantile Acquired Aphasia, Acquired Epileptic Aphasia, Aphasia with Convulsive Disorder
0
0
2008-12-26T16:45:11+00:00
2008-05-21T13:25:34+00:00
<p>Langerhans Cell Histiocytosis (<span class="caps">LCH</span>) is a rare disorder involving the langerhans cells, typically found bone marrow, which migrate throughout the body.</p>
<p>Langerhans Cell Histiocytosis (<span class="caps">LCH</span>) is a rare disorder involving the langerhans cells, typically found bone marrow, which migrate throughout the body.</p>
806
Langerhans Cell Histiocytosis
5
langerhans-cell-histiocytosis
0
2.0
http://www.orpha.net
Per 100,000 Population
LCH
0
1
2009-02-10T21:49:22+00:00
2008-05-21T13:25:34+00:00
<p>A Large or Giant Congenital Melanocytic Nevus (plural: Nevi) is a pigmented lesion, substantial in size, either present at birth or very shortly after birth (within 2 years). These rare large birthmarks carry a small risk of neurological (brain) complications, and are presumed to increase the incidence of skin cancer compared to people who don’t have them. Because people who have these “look different” psychological impacts can be great.</p>
<p>Something like one person in 100 is born with a small one of these. “Large” usually means it is bigger than 3cm across (about an inch) and “Giant” usually means it is larger than the hand of the person whose body it is on. These terms are not exact, and different doctors call them different things and use different words, depending on a lot of factors like if they are on the torso or on the head or on the arms/legs.</p>
<p>It’s important to know that there are not many doctors who know very much about these big birthmarks. It is best to find a doctor who has experience with large or giant nevi.</p>
873
803
Large Congenital Melanocytic Nevus
1
large-congenital-melanocytic-nevus
0
5.0
http://www.orpha.net
Per 100,000 Population
nevus, naevus, nevus, naevi, large nevus, large naevus, giant nevus, giant naevus, hairy nevus, hairy naevus, pigmented nevus, pigmented naevus, congenital nevus, congenital naevus
0
0
2010-02-18T16:53:56+00:00
2010-02-19T14:32:15+00:00
<p>Large Granular Lymphocytic Leukemia is a rae disease characterized by unexplained elevation in large granular lymphocytes in the blood.</p>
<p>Large Granular Lymphocytic Leukemia is a rae disease characterized by unexplained elevation in large granular lymphocytes in the blood.</p>
1469
Large Granular Lymphocytic Leukemia
1
large-granular-lymphocytic-leukemia
0
Per 100,000 Population
T-cell large granular lymphocyte leukemia, proliferation of large granular lymphocytes, LGL leukemia, Tγ-lymphoproliferative disorder, Subtype of: T cell leukemia, T-cell prolymphocytic leukemia, T-cell chronic lymphocytic leukemia
0
0
2010-02-19T14:32:15+00:00
2009-08-19T22:23:48+00:00
1426
Larsen Syndrome
0
larsen-syndrome
0
Per 100,000 Population
0
0
2009-08-19T22:23:48+00:00
2008-05-21T13:25:34+00:00
833
Laryngo-Tracheo-Esophageal Cleft
1
laryngo-tracheo-esophageal-cleft
0
1.5
http://www.orpha.net
Per 100,000 Population
Laryngotracheoesophageal Cleft, Laryngo Tracheo Esophageal Cleft
0
0
2009-08-05T03:18:21+00:00
2008-05-21T13:25:34+00:00
807
Lateral body wall complex
0
lateral-body-wall-complex
0
2.0
http://www.orpha.net
Per 100,000 Population
0
0
2008-05-21T13:25:34+00:00
2009-01-09T18:22:19+00:00
<p>Lateral Medullary Syndrome is a rare disorder characterized by difficulty swallowing or speaking due to dead tissue.</p>
<p>Lateral Medullary Syndrome is a rare disorder characterized by difficulty swallowing or speaking due to dead tissue.</p>
1310
Lateral Medullary Syndrome
0
lateral-medullary-syndrome
0
Per 100,000 Population
Wallenberg's Syndrome, Posterior Inferior Cerebellar Artery Syndrome, Wallenberg Syndrome
0
0
2009-01-09T18:22:19+00:00
2008-05-21T13:25:33+00:00
<p>Leber Hereditary Optic Neuropathy is an inherited degeneration of retinal ganglion cells leading to loss of central vision.</p>
<p>Leber Hereditary Optic Neuropathy is an inherited degeneration of retinal ganglion cells leading to loss of central vision.</p>
681
Leber Hereditary Optic Neuropathy
0
leber-hereditary-optic-neuropathy
0
6.5
http://www.orpha.net
Per 100,000 Population
LHON, Lebers Hereditary Optic Neuropathy, Leber Optic Atrophy, Leber's Hereditary Optic Neuropathy
Subtype of: mitochondrial cytopathies, mitochondrial cytopathy; Mitochondrial myopathy
0
0
2010-01-19T13:18:34+00:00
2008-05-21T13:25:34+00:00
<p>Leber’s Congenital Amaurosis is a rare inherited eye disorder.</p>
<p>Leber’s Congenital Amaurosis is a rare inherited eye disorder.</p>
780
Leber's Congenital Amaurosis
0
leber-s-congenital-amaurosis
0
2.5
http://www.orpha.net
Per 100,000 Population
LCA, Lebers Congenital Amaurosis, Amaurosis congenita of Leber, Amaurosis congenita de Leber
0
0
2010-02-11T19:08:05+00:00
2009-08-18T21:04:16+00:00
<p>Ledderhose’s Disease is a rare disorder consisting of non-malignant thickening of the feet’s deep connective tissue.</p>
<p>Ledderhose’s Disease is a rare disorder consisting of non-malignant thickening of the feet’s deep connective tissue.</p>
1409
Ledderhose's Disease
3
ledderhose-s-disease
0
Per 100,000 Population
Ledderhoses disease, Ledderhose disease, Morbus Ledderhose, plantar fibromatosis, and plantar aponeurosis
0
1
2009-08-18T22:14:44+00:00