Rare Disorders
CBEL
>> 132 Rare Disorders
Health
sites, last updated on 31 March 2008
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Progeria
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Progeria.ca: Too Young to be Old
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Hayleys Progeria Page
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NORD: Progeria, Hutchinson Gilford
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Progeria Family Circle
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Progeria Research Foundation, Inc.
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University of Washington: Werner S...
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Progeria Project Foundation
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Online Mendelian Inheritance in Ma...
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NORD: Werner Syndrome
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Hutchinson-Gilford Progeria Syndro...
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NCBI: Genes and Diseases
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Online Mendelian Inheritance in Ma...
Pierre Robin Syndrome
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Chases Story
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Pierre Robin Network
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Contact a Family: Pierre Robin Syn...
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NORD - Pierre Robin Syndrome
Phenylketonuria
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Firstplay Dietary Foods LTD
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Childrens PKU Network
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PKU-Info.org
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PKU Exchange
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Phenylketonuria
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Pediatric Oncall
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National PKU News
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Medline Plus: Phenylketonuria
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Genes and Diseases: Phenylketonuria
Triploidy
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Indian Pediatrics
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Sabrian Lynn Cox
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Texas Department of State Health S...
Rubinstein-Taybi Syndrome
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Rubinstein Taybi Syndrome Support ...
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Rubinstein-Taybi Syndrome
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Special Friends Foundation
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The CaF Directory
Melorheostosis
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Melorheostosis
Jacobsen Syndrome
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The Fragile WEB Site
Wegeners Granulomatosis
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Living with Wegeners Granulomatosis
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MedicineNet: Wegeners Granulomatosis
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Merck Manual: Wegeners Granulomatosis
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Wegeners Granulomatosis
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Wegeners Granulomatosis (WG)
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Wegeners Granulomatosis Association
Wegeners Granulomatosis
(part 2)
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Wegeners Granulomatosis Info
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Wegeners Granulomatosis Site
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WegenersNet
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Wegeners Granulomatosis, NIAID Fac...
Ollier Disease
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NORD: Ollier Disease
Pemphigus
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International Pemphigus Foundation
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The Pemphigus and Pemphigoid Society
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Pemphigus
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Pemphigus Research
Agnosia
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Prosopagnosia (Face Blindness)
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Visual Agnosia
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Agnosia
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Agnosia
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An Examination of Visual Agnosia
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Face Blind
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Prosopagnosia
VACTERL Association Personal Pages
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Alison Green
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Andrei Fagurel
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Benjamin Rockey
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Hannahs Story
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Leslie Sue Large
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Lily Hansen
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Ryans Life
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Schmidt Family Blog
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Zoe Lambert
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Aled Thomas Griffiths
Tyrosinemia
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NORD: Tyrosinemia, Hereditary
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Tyrosinemia
VACTERL Association
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The Vater Forum
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VATER Association
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EA/TEF Family Support Connection
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Tef/Vater International
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Tracheo-Oesophageal Fistula (TOF)
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VACTERL Association Support Group
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VACTERL Association Wiki
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VACTERL Network
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VACTERL or VATER Association
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VATER Association
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Cherubs
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Contact a Family
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European Organisation for Rare Dis...
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Fibrous Dysplasia Support Online
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Human Growth Foundation
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Information Centre for Rare Diseas...
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Kindler Syndrome
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National Organization for Rare Dis...
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Nomid /Cinca
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Office of Rare Diseases
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Tetrahydrobiopterin
Alström Syndrome
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Alström Syndrome
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Alström Syndrome UK Support Group
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NORD - Alström Syndrome
Barth Syndrome
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Barth Syndrome Foundation
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Clinical Mass Spectrometry Laboratory
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NINDS - Barth Syndrome Information
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The Complete Barth Syndrome Homepage
Aicardi Syndrome
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Aicardi Syndrome Foundation
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Contact a Family: Aicardi Syndrome
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Medline Plus: Aicardi Syndrome
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Megan
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National Library of Medicine: Aica...
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NINDS: Agenesis of the Corpus Callosum
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NINDS: Aicardi Syndrome
Cerebrocostomandibular Syndrome
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National Library of Medicine: cere...
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NORD - Cerebrocostomandibular Syndrome
Erythromelalgia
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Erythromelalgia (EM)
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NORD: Erythromelalgia
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The Erythromelalgia Association
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The Merck Manual: Erythromelalgia
Moyamoya
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E-Medicine: Moyamoya Disease
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Moyamoya Disease
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Moyamoya Disease
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Moyamoya Disease
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NINDS: Moyamoya Disease
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NORD: Moyamoya Disease
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Pediatric Oncall
Pemphigoid
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EMedicine: Bullous pemphigoid
Cleidocranial Dysplasia
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A Natural History of Cleidocranial...
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MedicineNet.com: Cleidocranial Dys...
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National Library of Medicine: Clei...
Cystinosis
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Cornea and External Diseases - Cys...
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Cystinosis Central
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Cystinosis Clinical Resources
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Cystinosis Foundation
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Cystinosis Research Foundation
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Cystinosis Research Network
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EyeRounds.org: Cystinosis
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The Cystinosis Foundation UK
Degos
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NORD: Degos Disease
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EMedicine - Degos Disease :
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Degos Patients Support Network
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Doctors Doctor: Degos Disease
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