Genetic Disorders
Alliance of Genetic
Support Groups
Alpha-1 Antitrypsin Deficiency
(A1AD) Association
Alpha One Foundation
Alliance of Genetic
Support Groups
Bannayan
Zonana Syndrome
Blazing a Genetic
Trail
Canadian Associaton of
Genetic Counsellors (CAGC)
Center for Inherited
Disease Research - Johns Hopkins University
Center for
Inherited Disorders of Energy Metabolism (CIDEM) - Case Western Reserve
University
CFC
Family Network
Chromosome 9P- Network
Clinical
Genetics: A Self Study for Health Care Provider
Dubowitz Syndrome
Information & Parent Support
Familial
Hypercholesterolemia treatment, prevention, and more.
Genetic
Disease Information
Genetic
Disorders treatment, prevention. - Information on treatment, prevention,
diagnosis, and support groups.
Genetic Information and
Patient Services, Inc (GAPS) - Links to online definitions, information
sites, and support groups for genetic disorders and birth defects.
G6PD Deficiency - G6PD
deficiency is the most common human enzyme deficiency in the world; it affects
an estimated 400 million people worldwide.
GeneCardsGeneClinics
Genes and
Disease
Genetic Disorders
& Birth Defects - Sri Lanka Collection
Genetics Education and
Counseling Program -
Hed Foundation
Hereditary Disease
Foundation
Human Gene
Mutation Database
Infantile
Refsum's Disease
International
Organization of Glutaric Acidemia
International Society
for Mannosidosis & Related Diseases
Hereditary Disease
Foundation
Human
Genomics
International Joseph Disease
Foundation
International Society
for Mannosidosis & Related Diseases
Kimball Genetics -
Genetic Testing in Preventive Medicine
Late Onset
Congenital Adrenal Hyperplasia
Lowe Syndrome
Association
McArdle's
Disease Information Source
Meckel
Gruber Syndrome: In Memorium for Max
Medical Genetics has a homepage
Nail Patella
Syndrome
New Zealand Lysosomal Storage
Diseases Support Group
OMIM Home Page --
Online Mendelian Inheritance in Man
Primary Ciliary Dyskinesia
Progeria Research
Foundation, Inc.
S.O.F.T. - A support
organisation for parents of infants with Trisomy 13 & 18 and other related
disorders.
Spiral Notebook: Short
takes on CPT deficiency
Strickler
Family Homepage
Sundowner
- Information on Familial Mediterranean Fever and other diseases that affect
people of Melungeon descent in America.
Taryn's
World: About Switches - Personal page for kids and parents about genetic
disorders, especially mannosidosis.
Urea Cycle Disorders
Lysosomal
Storage Diseases: A Family Sourcebook
Medical Genetics
Mucolipidosis IV Foundation
Murdoch Institute
National Association for
Psuedoxanthoma Elasticum
National Dysautonomia Research
Foundation
National Society of Genetic
Counselors
Neurogenetics
- Massachusetts General Hospital
Office of Genetics and
Disease Prevention
OMIM: Online
Mendelian Inheritance in Man
Pseudoxanthoma
Elasticum (PXE)
Public Health Genetics
Society
Purine
Metabolic Patients' Association - charity supporting families with members
suffering from purine metabolic diseases.
Rare
Genetic Diseases in Children
Schiz
Kidz Buddies
Smith-Lemli-Opitz
Syndrome
Spiral Notebook:
Carnitine Palmitoyl Transferase Deficiency
Tetrasomy 18p
Unique
Velo-Cardio-Facial
Syndrome
Xeroderma Pigmentosum Society
- provides information on the disease also known as XP
