Please see also specific disorder or condition in the alphabetical listings.
This page was last updated on July 10th, 2008
This page was last updated on July 10th, 2008
Genetic Disorders (from Conditions and Diseases)
Canadian Content » Health » Conditions_and_Diseases » Genetic_Disorders »
XLH Network
Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.
Your Genes, Your Health
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
Genetic and Rare Conditions
Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
IMMD Institute of Medical Molecular Diagnostics Ltd.
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.
Primary Ciliary Dyskinesia
Information on a rare congenital disease.
The UDGD Spot
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.
Dr. Greene's HouseCalls
A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.
Genetic Disorders: The Links to Diet
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.
Gene Clinics
Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
Blepharophimosis Ptosis Epicanthus Inversus Syndrome
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.
Washington University in St Louis
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.
Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
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.
Information on a rare congenital disease.
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.
A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.
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.
Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
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.
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.
Conditions and Diseases >> Genetic Disorders yielded other results on Canadian Content:
Mobile phones boost brain tumor risk
Originally Posted by Niflmir The funny thing is that the scientists conclude the exact opposite of
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Stephen Harper vows free vote on gay marriage
December 3rd, 2005, 01:34 PM That pretty much speaks for itself, Colpy...Conservatives don't care a
December 3rd, 2005, 01:34 PM That pretty much speaks for itself, Colpy...Conservatives don't care a
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The Purpose of Pain Philosophy Discussion
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March 13th, 2007, 02:17 PM My family has a genetic disposition to diabetes on my mother's side... H
March 13th, 2007, 02:17 PM My family has a genetic disposition to diabetes on my mother's side... H
Designer BABIES !!!
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- Aarskog Syndrome
- Aase Syndrome
- Ablepharon-Macrostomia Syndrome
- Acoustic Neuroma@
- Adie Syndrome@
- Adrenal Hyperplasia@
- Adrenoleukodystrophy@
- Aicardi Syndrome@
- Alagille Syndrome
- Albinism@
- Alkaptonuria
- Alopecia Areata@
- Alpha-1 Antitrypsin Deficiency
- Alstrom Syndrome@
- Angelman Syndrome@
- Apert Syndrome@
- Arthrogryposis@
- Ataxia@
- Autism@
- Bardet-Biedl Syndrome@
- Barth Syndrome@
- Batten
- Beckwith-Wiedemann Syndrome
- Canavan@
- Celiac@
- Cerebrocostomandibular Syndrome@
- Charcot-Marie-Tooth Disease@
- Cleidocranial Dysplasia@
- Cockayne Syndrome@
- Coffin Lowry Syndrome
- Congenital Cardiovascular Disorders@
- Congenital Heart Disease@
- Congenital Musculoskeletal Disorders@
- Congenital Neurological Disorders@
- Congenital Pain Insensitivity@
- Congenital Urological Disorders@
- Cornelia De Lange Syndrome@
- Costello Syndrome
- Cowden Syndrome
- Craniofrontonasal Dysplasia
- Cri du Chat Syndrome@
- Crigler-Najjar Syndrome
- Cystic Fibrosis
- Cystinosis@
- DiGeorge Syndrome
- Down Syndrome
- Dubowitz Syndrome
- Dwarfism@
- Ectodermal Dysplasia
- Ehlers-Danlos Syndrome@
- Factor V Leiden@
- Familial Dysautonomia@
- Familial Erythromelalgia@
- Familial Hypercholesterolemia
- Fanconi Anemia@
- Fatty Oxidation
- Floating-Harbor Syndrome
- Fragile X Syndrome
- Friedreich Ataxia@
- Galactosemia@
- Gaucher's@
- Gene Therapy@
- Genetic Testing and Counseling@
- Genetics Education@
- Glutaricaciduria
- Glycogen Storage Disease Type II@
- Hailey-Hailey Disease
- Hallervorden-Spatz Syndrome@
- Hemihypertrophy
- Hemochromatosis
- Hemophilia@
- Hereditary Angioedema
- Hereditary Spastic Paraplegia
- Homocystinuria@
- Human Genetics@
- Huntington's@
- Hydrocephalus@
- Incontinentia Pigmenti
- Jacobsen Syndrome@
- Joubert Syndrome
- Klinefelter Syndrome
- Klippel-Feil Syndrome
- Langer-Giedion Syndrome
- Laurence-Moon Syndrome
- Leigh's
- Lesch-Nyhan Syndrome
- Leukodystrophy
- Lissencephaly
- Lowe Syndrome
- Lymphedema
- Machado-Joseph
- Mannosidosis
- Marfan Syndrome
- McArdle's
- Meckel-Gruber Syndrome
- Menkes' Syndrome
- Mobius Syndrome
- Multiple Hereditary Exostoses
- Muscular Dystrophies
- Myotonic Dystrophy
- Nail Patella Syndrome
- Narcolepsy
- Neurofibromatosis
- Niemann-Pick
- Noonan Syndrome
- Opitz Syndrome
- Organizations
- Osteogenesis Imperfecta
- Pallister Killian Mosaic Syndrome
- Pallister-Hall Syndrome
- Personal Pages
- Phenylketonuria
- Polycystic Kidney
- Popliteal Pterygium Syndrome
- Porphyrias
- Prader-Willi Syndrome
- Progeria
- Propionic Acidemia
- Proteus Syndrome
- Prune Belly Syndrome
- Pseudoxanthoma Elasticum
- Refsum's
- Retinoblastoma
- Rett's Syndrome
- Robinow Syndrome
- Rubinstein-Taybi Syndrome
- Russell Silver Syndrome
- Sanfilippo Syndrome
- Schizencephaly
- Shwachman Syndrome
- Sickle Cell
- Smith Lemli Opitz Syndrome
- Smith-Magenis Syndrome
- Soto's Syndrome
- Spinal Muscular Atrophy
- Stickler's Syndrome
- Sturge-Weber Syndrome
- Support Groups
- Tay-Sachs
- Thalassemia
- Thrombocytopenia Absent Radius Syndrome
- Tourette Syndrome
- Treacher Collins Syndrome
- Tuberous Sclerosis
- Turner Syndrome
- Tyrosinemia
- Urea Cycle
- Usher Syndrome
- VATER Syndrome
- Velo-Cardio-Facial Syndrome
- Von Hippel-Lindau
- WAGR Syndrome
- Waardenburg Syndrome
- Weaver Syndrome
- Williams Syndrome
- Wilson's Disease
- Xeroderma Pigmentosum
- Zellweger Syndrome
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