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Home : Conditions and Diseases : Genetic Disorders
Alagille Syndrome Noonan Syndrome
Alkaptonuria Opitz Syndrome
Batten Organizations
Beckwith-Wiedemann Syndrome Personal Pages
Costello Syndrome Prader-Willi Syndrome
Crigler-Najjar Syndrome Propionic Acidemia
Cystic Fibrosis Proteus Syndrome
Down Syndrome Prune Belly Syndrome
Ectodermal Dysplasia Pseudoxanthoma Elasticum
Epidermolysis Bullosa Robinow Syndrome
Fatty Oxidation Sanfilippo Syndrome
Fragile X Syndrome Shwachman Syndrome
Glutaricaciduria Sirenomelia
Hemochromatosis Smith-Magenis Syndrome
Hereditary Angioedema Soto's Syndrome
Hereditary Spastic Paraplegia Sturge-Weber Syndrome
Joubert Syndrome Turner Syndrome
Klinefelter Syndrome Urea Cycle
Laurence-Moon Syndrome Velo-Cardio-Facial Syndrome
Lowe Syndrome Von Hippel-Lindau
Machado-Joseph Weaver Syndrome
Mannosidosis Williams Syndrome
Nail Patella Syndrome Xeroderma Pigmentosum
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.
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 Center For Jewish Genetics Disorders
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.
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.
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