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Thursday, Nov 20, 2008 | 09:08 AM
Madisons Foundation - Moms And Dads In Search Of Needed Support
m-Power® Rare Pediatric Disease Database
Full disease list by letter:
3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | X | Y | Z | All
3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | X | Y | Z | All
Nijmegen Breakage Syndrome
Berlin Breakage Syndrome, Seemanova Syndrome
Nijmegen breakage syndrome is a rare, inherited genetic disorder that is characterized by a small head, growth retardation, recurrent respiratory infections, premature ovarian failure in females, and an increased risk of developing childhood cancer (primarily lymphomas).
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Non-Hodgkin's Lymphoma (NHL)
Non-Hodgkin’s lymphoma (NHL) is a type of tumor of the lymphatic system, and is the sixth most common cancer in the United States. The lymphatic system is part of the body’s immune system, and is involved in the production and transport of lymphocytes. Lymphocytes are cells that produce antibodies that attack foreign substances like viruses and bacteria. There are 20 distinct types of non-Hodgk...
Noonan Syndrome
Noonan’s Syndrome is a genetic condition that affects the heart, growth, mental and physical development, and clotting of the blood.
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Norrie Disease
X-linked Familial Exudative Vitreoretinopathy, Atrophia Bulborum Hereditaria, Andersen-Warburg disea
Norrie disease is a rare, inherited genetic disorder that results in progressive blindness, deafness, and mental retardation in children. It presents in several forms ranging from those with mild visual problems to total blindness and deafness in early childhood. ...