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Aicardi Syndrome (1)
Alstr?m Syndrome (2)
Barth Syndrome (1)
Cystinosis (2)
Degos (1)
Erythromelalgia (1)
Melorheostosis (1)
Moyamoya (1)
Pemphigus (2)
Phenylketonuria (3)
Pierre Robin Syndrome (2)
Progeria (3)
Rubinstein-Taybi Syndrome (2)
Wegeners Granulomatosis (2)
Listing (s)
Cherubs details
A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.
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Contact a Family details
Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK.
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Human Growth Foundation details
Information about growth-related disorders through education, research, and advocacy. Member driven organization.
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Lymphangiomatosis and Gorham's Vanishing Bone Disease details
Provides general information and a personal account, including pictures and X-rays.
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National Organization for Rare Disorders, Inc. details
Information about NORD, its programs, special events and the variety of services offered.
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Tetrahydrobiopterin details
Information on structure, biosynthesis and pathophysiology of BH4 and tetrahydrobiopterin deficiency.
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XLH Network details
Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.
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