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Additional Resources
(not subjected to our MD rating):

REFERENCE:
Medifocus subject reports.
,

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NutriCounter.
, Vitality Medical.
, Wright Stuff diabetes.
,

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NutriCounter.
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DrugStore.
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Vitality Medical for patients.
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FamilyMobility electric wheelchairs, scooters, lift chairs, ramps, lifts (Medicaire, $75 coupon).
, Professional:
Vitality Medical.
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Premier Fitness.
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International Jock.
, Post-Natal:
BodyTrends.
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Gold Violin Gadgets.
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General:
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Keen pregnancy talk.
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DentalPlans.
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Avon.
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LifeSign Quit Smoking.
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STORES:
General:
DrugStore.
, Gaiam Naturals.
, Specialty:
Abundant Earth Organic.
,

WELLNESS:
Rubs.org massage.
, SpaWish.
,

Home > Health > Conditions_and_Diseases > Genetic_Disorders


See also:
Health: Conditions_and_Diseases: Genetic_Disorders: Zellweger_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Organizations
Health: Conditions_and_Diseases: Genetic_Disorders: Propionic_Acidemia
Health: Conditions_and_Diseases: Genetic_Disorders: Dubowitz_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Mobius_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Pallister-Hall_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Incontinentia_Pigmenti
Health: Conditions_and_Diseases: Genetic_Disorders: Meckel-Gruber_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Crigler-Najjar_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: DiGeorge_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Floating-Harbor_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Waardenburg_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Hailey-Hailey_Disease
Health: Conditions_and_Diseases: Genetic_Disorders: Noonan_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Thrombocytopenia_Absent_Radius_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Xeroderma_Pigmentosum
Health: Conditions_and_Diseases: Genetic_Disorders: Popliteal_Pterygium_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Prune_Belly_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Ablepharon-Macrostomia_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Aarskog_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Proteus_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Opitz_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Coffin_Lowry_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Hemochromatosis
Health: Conditions_and_Diseases: Genetic_Disorders: Pallister_Killian_Mosaic_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Craniofrontonasal_Dysplasia
Health: Conditions_and_Diseases: Genetic_Disorders: Fragile_X_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Glutaricaciduria
Health: Conditions_and_Diseases: Genetic_Disorders: Robinow_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Velo-Cardio-Facial_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Alkaptonuria
Health: Conditions_and_Diseases: Genetic_Disorders: Russell_Silver_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Down_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Nail_Patella_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Hereditary_Spastic_Paraplegia
Health: Conditions_and_Diseases: Genetic_Disorders: Prader-Willi_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Lesch-Nyhan_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Williams_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Ectodermal_Dysplasia
Health: Conditions_and_Diseases: Genetic_Disorders: Turner_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Lowe_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Pseudoxanthoma_Elasticum
Health: Conditions_and_Diseases: Genetic_Disorders: Smith-Magenis_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Machado-Joseph
Health: Conditions_and_Diseases: Genetic_Disorders: Hemihypertrophy
Health: Conditions_and_Diseases: Genetic_Disorders: Batten
Health: Conditions_and_Diseases: Genetic_Disorders: McArdle's
Health: Conditions_and_Diseases: Genetic_Disorders: Smith_Lemli_Opitz_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Shwachman_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Laurence-Moon_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Alpha-1_Antitrypsin_Deficiency
Health: Conditions_and_Diseases: Genetic_Disorders: Sturge-Weber_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Personal_Pages
Health: Conditions_and_Diseases: Genetic_Disorders: Cowden_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Beckwith-Wiedemann_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Soto's_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Joubert_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Familial_Hypercholesterolemia
Health: Conditions_and_Diseases: Genetic_Disorders: Alagille_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Von_Hippel-Lindau
Health: Conditions_and_Diseases: Genetic_Disorders: Costello_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Usher_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Klinefelter_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Cystic_Fibrosis
Health: Conditions_and_Diseases: Genetic_Disorders: Hereditary_Angioedema
Health: Conditions_and_Diseases: Genetic_Disorders: Weaver_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Fatty_Oxidation
Health: Conditions_and_Diseases: Genetic_Disorders: Sanfilippo_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Aase_Syndrome
Health: Conditions_and_Diseases: Genetic_Disorders: Schizencephaly
Health: Conditions_and_Diseases: Genetic_Disorders: Mannosidosis
Health: Conditions_and_Diseases: Genetic_Disorders: Urea_Cycle

1.Washington University in St Louis
line
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.
URL:http://hematology.wustl.edu/registry

2.Rare Genetic Diseases In Children
line
A layman's guide to genetic diseases, and a comprehensive resource for families on lysosomal storage diseases.
URL:http://mcrcr2.med.nyu.edu/murphp01/homenew.htm

3.Respiratory Syndromes Associated with Congenital Abnormalities of Mucociliary Clearance
line
A resource providing information for physicians and patients on laboratory analyses of Primary Ciliary Dyskinesia, Immotile Cilia Syndrome, and Kartagener's Syndrome.
URL:http://pediatrics.med.unc.edu/id/pcd/

4.Your Genes, Your Health
line
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
URL:http://vector.cshl.org/ygyh

5.The UDGD Spot
line
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.
URL:http://www.camp-a-roo.com/UDGD/

6.Dr. Greene's HouseCalls
line
A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.
URL:http://www.drgreene.com/html/21614.html

7.Gene Clinics
line
Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
URL:http://www.geneclinics.org

8.Genetic and Rare Conditions Site
line
Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
URL:http://www.kumc.edu/gec/support/

9.Genetic Disorders: The Links to Diet
line
Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy and homocystinuria and cystic fibrosis.
URL:http://www.mindspring.com/~sandysimmons/genetic_disorders.html

10.Primary Ciliary Dyskinesia
line
Information on a rare congenital disease.
URL:http://www.p-c-d.org/en/

11.XLH Network
line
Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.
URL:http://www.xlhnetwork.org




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