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Genetic Disorders (10) - order by Newest
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Aarskog Syndrome
Aase Syndrome
Ablepharon-Macrostomia Syndrome
Alagille Syndrome
Alkaptonuria
Alpha-1 Antitrypsin Deficiency
Batten
Beckwith-Wiedemann Syndrome
Coffin Lowry Syndrome
Costello Syndrome
Cowden Syndrome
Craniofrontonasal Dysplasia
Crigler-Najjar Syndrome
Cystic Fibrosis
DiGeorge Syndrome
Down Syndrome
Down's Syndrome
Dubowitz Syndrome
Ectodermal Dysplasia
Epidermolysis Bullosa
Familial Hypercholesterolemia
Fatty Oxidation
Floating-Harbor Syndrome
Fragile X Syndrome
Glutaricaciduria
Hailey-Hailey Disease
Hemihypertrophy
Hemochromatosis
Hereditary Angioedema
Hereditary Spastic Paraplegia
Incontinentia Pigmenti
Joubert Syndrome
Klinefelter Syndrome
Laurence-Moon Syndrome
Lesch-Nyhan Syndrome
Lowe Syndrome
Machado-Joseph
Mannosidosis
McArdle's
Meckel-Gruber Syndrome
Mobius Syndrome
Nail Patella Syndrome
Noonan Syndrome
Opitz Syndrome
Pallister Killian Mosaic Syndrome
Pallister-Hall Syndrome
Personal Pages
Popliteal Pterygium Syndrome
Prader-Willi Syndrome
Propionic Acidemia
Proteus Syndrome
Prune Belly Syndrome
Pseudoxanthoma Elasticum
Robinow Syndrome
Russell Silver Syndrome
Sanfilippo Syndrome
Schizencephaly
Shwachman Syndrome
Sirenomelia
Smith Lemli Opitz Syndrome
Smith-Magenis Syndrome
Soto's Syndrome
Sturge-Weber Syndrome
Thrombocytopenia Absent Radius Syndrome
Trichothiodystrophy
Turner Syndrome
Urea Cycle
Usher Syndrome
Velo-Cardio-Facial Syndrome
Von Hippel-Lindau
Waardenburg Syndrome
Weaver Syndrome
Williams Syndrome
Xeroderma Pigmentosum
Zellweger Syndrome
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�
New Scientist: Heroin Addiction Gene Identified and Blocked
Description:
Scientists have not only identified a critical gene involved in heroin addiction relapse, but they have also successfully blocked it, eliminating cravings for the drug.
(May 31, 2005)
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Added:
10/13/2002
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�
Your Genes, Your Health
Description:
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
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76
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Added:
10/12/2002
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�
Washington University in St Louis
Description:
Family resource for individuals with Papillon Lefevre, Haim-Munk Syndrome and Prepubertal Periodontis. Interested families may participate in a registry dedicated to learning about the natural history of these three conditions.
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180
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10/11/2002
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�
The UDGD Spot
Description:
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.
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108
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10/10/2002
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�
Primary Ciliary Dyskinesia
Description:
Information on a rare congenital disease.
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96
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10/9/2002
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IMMD Institute of Medical Molecular Diagnostics Ltd.
Description:
The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood.
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72
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10/8/2002
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Genetic Disorders: The Links to Diet
Description:
Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis.
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112
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10/7/2002
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The Center For Jewish Genetics Disorders
Description:
A critical effort to provide public and professional education for many of the identified Jewish genetic disorders. Find info on screening and counseling, advocacy, events and community resources.
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86
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10/6/2002
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Blepharophimosis Ptosis Epicanthus Inversus Syndrome
Description:
The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder.
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Added:
10/5/2002
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�
A3243G
Description:
Explains a gene defect which causes several diseases including Maternally Inherited Diabetes with Deafness. Features a newsletter, forum and definitions.
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144
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Added:
10/4/2002
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