2008-05-21T13:25:35+00:00
<p>Naegeli–Franceschetti–Jadassohn Syndrome is a rare form of ectodermal dysplasia characterized by reticular skin pigmentation, diminished function of the sweat glands, the absence of teeth and the thickening of the skin of the palms and soles.</p>
<p>Naegeli–Franceschetti–Jadassohn Syndrome is a rare form of ectodermal dysplasia characterized by reticular skin pigmentation, diminished function of the sweat glands, the absence of teeth and the thickening of the skin of the palms and soles.</p>
1036
Naegeli-Franceschetti-Jadassohn Syndrome
0
naegeli-franceschetti-jadassohn-syndrome
0
0.04
http://www.orpha.net
Per 100,000 Population
Chromatophore nevus of Naegeli, Naegeli Franceschetti Jadassohn syndrome, Subset of ectodermal dysplasia
0
0
2010-02-10T21:20:56+00:00
<p>Genetic mutation of the gene LMX1B on chromosome 9q34</p>
2008-05-21T13:25:34+00:00
<p>Nail-Patella Syndrome is a rare genetic disorder characterized by hypoplastic or absent patellae, dystrophic nails, dysplasia of the elbows, iliac horns, clubbed feet, glaucoma and kidney disease.</p>
<p>Nail-Patella Syndrome is a rare genetic disorder characterized by hypoplastic or absent patellae, dystrophic nails, dysplasia of the elbows, iliac horns, clubbed feet, glaucoma and kidney disease.</p>
808
Nail-Patella Syndrome
3
nail-patella-syndrome
0
2.0
http://www.orpha.net
Per 100,000 Population
Iliac Horn Syndrome, Hereditary Onychoostedysplasia, Fong Disease, Turner-Kiser Syndrome, Nail Patella Syndrome, NPS, HOOD
0
1
2008-12-10T22:47:17+00:00
2008-05-21T13:25:32+00:00
<p>Narcolepsy is a neurological condition most characterized by Excessive Daytime Sleepiness.</p>
<p>Narcolepsy is a neurological condition most characterized by Excessive Daytime Sleepiness.</p>
525
Narcolepsy
1
narcolepsy
0
49.0
http://www.orpha.net
Per 100,000 Population
Irresistible Sleepiness, Cataplexy, Onset of Sleep in Desynchronized Phase, Narcolepsy-Cataplexy, Gelineau Disease
0
0
2009-01-12T23:02:23+00:00
2008-05-21T13:25:33+00:00
650
NARP syndrome
0
narp-syndrome
0
8.5
http://www.orpha.net
Per 100,000 Population
0
1
2008-05-21T13:25:33+00:00
2008-05-21T13:25:34+00:00
<p>Nemaline Myopathy is a rare neuromuscular disorder.</p>
<p>Nemaline Myopathy is a rare neuromuscular disorder.</p>
879
Nemaline Myopathy
0
nemaline-myopathy
0
1.0
http://www.orpha.net
Per 100,000 Population
rod myopathy, nemaline rod myopathy
0
1
2009-06-12T18:27:00+00:00
2008-05-21T13:25:35+00:00
<p>Neonatal Diabetes Mellitus is a genetic form of diabetes resulting in the congenital impairment of insulin release.</p>
<p>Neonatal Diabetes Mellitus is a genetic form of diabetes resulting in the congenital impairment of insulin release.</p>
976
Neonatal Diabetes Mellitus
1
neonatal-diabetes-mellitus
0
0.2
http://www.orpha.net
Per 100,000 Population
Permanent neonatal diabetes mellitus
0
0
2009-10-06T14:06:57+00:00
2008-12-18T19:43:04+00:00
<p>Neonatal Onset Multisystem Inflammatory Disease is a rare genetic disorder which causes inflammation in multiple parts of the body.</p>
<p>Neonatal Onset Multisystem Inflammatory Disease is a rare genetic disorder which causes inflammation in multiple parts of the body.</p>
1275
Neonatal Onset Multisystem Inflammatory Disease
6
neonatal-onset-multisystem-inflammatory-disease
0
100.0
http://www.orpha.net/data/patho/Pro/en/CINCA-FRenPro3395.pdf
Cases
NOMID, Chronic Neurologic Cutaneous and Articular Syndrome, CINCA, Cryopyrin-Associated Periodic Syndromes, CAPS, Chronic Infantile Neurological, Cutaneous and Articular Syndrome
0
0
2009-02-08T06:55:03+00:00
2008-05-21T13:25:34+00:00
<p>Diabetes insipidus is a disorder characterized by excretion of large amounts of diluted urine. Nephrogenic diabetes insipidus is cuased by the kidney’s inabilityto respond normally to <span class="caps">ADH</span>.</p>
<p>Diabetes insipidus is a disorder characterized by excretion of large amounts of diluted urine. Nephrogenic diabetes insipidus is cuased by the kidney’s inabilityto respond normally to <span class="caps">ADH</span>.</p>
923
Nephrogenic diabetes insipidus
2
nephrogenic-diabetes-insipidus
0
0.5
http://www.orpha.net
Per 100,000 Population
0
0
2008-08-02T20:17:37+00:00
2009-03-23T15:34:31+00:00
<p>Nephrogenic Systemic Fibrosis is a rare disorder involving fibrosis of skin, joints, eyes, and internal organs.</p>
<p>Nephrogenic Systemic Fibrosis is a rare disorder involving fibrosis of skin, joints, eyes, and internal organs.</p>
1372
Nephrogenic Systemic Fibrosis
0
nephrogenic-systemic-fibrosis
0
Per 100,000 Population
NSF, Nephrogenic fibrosing dermopathy
0
0
2009-03-23T15:34:31+00:00
2008-11-07T15:46:35+00:00
<p>Nerve Entrapment is a disorder that occurs when nerves become compressed or entrapped at various regions of the extremities.</p>
<p>Nerve Entrapment is a disorder that occurs when nerves become compressed or entrapped at various regions of the extremities.</p>
1241
Nerve Entrapment
1
nerve-entrapment
0
Per 100,000 Population
carpal tunnel syndrome, cubital tunnel, Guyon canal, meralgia paresthetica, Tarsal tunnel syndrome,
0
0
2008-11-07T15:46:35+00:00
2008-05-21T13:25:34+00:00
841
Netherton Syndrome
0
netherton-syndrome
0
1.35
http://www.orpha.net
Per 100,000 Population
Netherton disease
0
0
2009-09-24T13:08:48+00:00
2008-05-21T13:25:33+00:00
636
Neuroblastoma
3
neuroblastoma
0
10.0
http://www.orpha.net
Per 100,000 Population
0
1
2009-07-03T03:07:41+00:00
2008-05-21T13:25:32+00:00
<p>Neurofibromatosis Type 1 is a rare inherited disease characterized by neurologic and dermatologic lesions.</p>
<p>Neurofibromatosis Type 1 is a rare inherited disease characterized by neurologic and dermatologic lesions.</p>
560
Neurofibromatosis Type 1
7
neurofibromatosis-type-1
0
25.0
http://www.orpha.net
Per 100,000 Population
von Recklinghausen Syndrome, Neurofibromatosis Type I, NF I
0
0
2008-09-12T16:57:35+00:00
2008-05-21T13:25:34+00:00
<p>Neurofibromatosis Type 2 is rare inherited genetic disorder characterized by non-malignant brain tumours in the vestibulocochlear nerve.</p>
<p>Neurofibromatosis Type 2 is rare inherited genetic disorder characterized by non-malignant brain tumours in the vestibulocochlear nerve.</p>
924
Neurofibromatosis Type 2
3
neurofibromatosis-type-2
0
0.5
http://www.orpha.net
Per 100,000 Population
MISME Syndrome, Multiple Inherited Schwannomas, Meningiomas, and Ependymomas, Neurofibromatosis Type II, NF-2, NF2
0
0
2008-08-31T15:40:40+00:00
2008-05-21T13:25:33+00:00
<p>Neuropathy Hereditary with Liability to Pressure Palsies is a disorder in which the peripheral nerves are unusually sensitive to pressure.</p>
<p>Neuropathy Hereditary with Liability to Pressure Palsies is a disorder in which the peripheral nerves are unusually sensitive to pressure.</p>
643
Neuropathy Hereditary with Liability to Pressure Palsies
5
neuropathy-hereditary-with-liability-to-pressure-palsies
0
9.0
http://www.orpha.net
Per 100,000 Population
0
0
2009-09-29T19:53:13+00:00