Health and Fitnees Information - Conditions and Diseases : Genetic Disorders

WEBSITE SEARCH

Find health resources in your area. Directory of links to thousands of health sites...

Advanced Search

CHILD HEALTH

Comprehensive resources and references about common children's health issues, with parenting and medical information.

CONDITIONS AND DISEASES

Discover symptoms, treatment options, and support for the common and rare physical and mental illnesses that afflict us all.

MENTAL HEALTH

Provide you comprehensive Mental Health and Mental Illness information on topics like Depression, Bipolar, Suicide, Anxiety, Schizophrenia, ...

REPRODUCTIVE HEALTH

Works to ensure universal access to reproductive health, including family planning and sexual health to all couples and individuals. ...

WOMEN'S HEALTH

Women's health information, tips, and research from the Centers for Disease Control and Prevention.

Genetic Disorders

Genetic Disorders Subcategories

Aarskog Syndrome	Mannosidosis
Aase Syndrome	McArdles
Ablepharon-Macrostomia Syndrome	MEB Disease
Alagille Syndrome	Meckel-Gruber Syndrome
Alfis Syndrome	Mobius Syndrome
Alkaptonuria	Mulibrey Nanism
Alpha-1 Antitrypsin Deficiency	Nail Patella Syndrome
Batten Disease	Nasu-Hakola Disease
Beckwith-Wiedemann Syndrome	Noonan Syndrome
Bloom Syndrome	Opitz Syndrome
Branchio-Oto-Renal Syndrome	Organizations
Coffin Lowry Syndrome	Pallister Killian Mosaic Syndrome
Cohen Syndrome	Pallister-Hall Syndrome
Costello Syndrome	Personal Pages
Cowden Syndrome	Popliteal Pterygium Syndrome
Craniofrontonasal Dysplasia	Prader-Willi Syndrome
Crigler-Najjar Syndrome	Propionic Acidemia
Currarino Syndrome	Proteus Syndrome
Cystic Fibrosis	Prune Belly Syndrome
DiGeorge Syndrome	Pseudoxanthoma Elasticum
Down Syndrome	RAPADILINO Syndrome
Dubowitz Syndrome	Robinow Syndrome
Ectodermal Dysplasia	Russell Silver Syndrome
Epidermolysis Bullosa	Sanfilippo Syndrome
Familial Hypercholesterolemia	Schizencephaly
Fatty Oxidation	Shwachman Syndrome
Floating-Harbor Syndrome	Sirenomelia
Fragile X Syndrome	Smith Lemli Opitz Syndrome
Gilberts Syndrome	Smith-Magenis Syndrome
Glutaricaciduria	Sotos Syndrome
Hailey-Hailey Disease	Sturge-Weber Syndrome
Hemihypertrophy	Thrombocytopenia Absent Radius Syndrome
Hemochromatosis	Trichothiodystrophy
Hereditary Angioedema	Turner Syndrome
Hereditary Spastic Paraplegia	Urea Cycle
Hydrolethalus Syndrome	Usher Syndrome
Incontinentia Pigmenti	Velo-Cardio-Facial Syndrome
Joubert Syndrome	Von Hippel-Lindau
Klinefelter Syndrome	Waardenburg Syndrome
Laurence-Moon Syndrome	Weaver Syndrome
Lesch-Nyhan Syndrome	Williams Syndrome
Loeys-Dietz Syndrome	Wolf-Hirschhorn Syndrome
Lowe Syndrome	Xeroderma Pigmentosum
Machado-Joseph	Zellweger Syndrome

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.

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.

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.

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.

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.

What malformation did El Greco paint?
El Greco�s faces are modelled on a child with a distinctive malformation. But what condition is it?

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.

New Scientist: Heroin Addiction Gene Identified and Blocked
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)

Homepage | Add site | Contact

Search | Site Map