A health medical information Conditions and Diseases

Aarskog Syndrome (4)
Aase Syndrome (3)
Ablepharon-Macrostomia Syndrome (3)
Acoustic Neuroma@ (8)
Adie Syndrome@ (3)
Adrenal Hyperplasia@ (5)
Adrenoleukodystrophy@ (4)
Aicardi Syndrome@ (6)
Alagille Syndrome (4)
Albinism@ (9)
Alfi's Syndrome (2)
Alkaptonuria (3)
Alopecia Areata@ (10)
Alpha-1 Antitrypsin Deficiency (11)
Alstrom Syndrome@ (3)
Angelman Syndrome@ (18)
Apert Syndrome@ (10)
Arthrogryposis@ (27)
Aspartylglucosaminuria@ (3)
Ataxia@ (6)
Autism@ (471)
Bardet-Biedl Syndrome@ (3)
Barth Syndrome@ (3)
Batten Disease (7)
Beckwith-Wiedemann Syndrome (6)
Bloom Syndrome (4)
Branchio-Oto-Renal Syndrome (4)
Canavan@ (3)
Celiac@ (53)
Cerebrocostomandibular Syndrome@ (2)
Charcot-Marie-Tooth Disease@ (7)
Choroideremia@ (3)
Cleidocranial Dysplasia@ (3)
Cockayne Syndrome@ (3)
Coffin Lowry Syndrome (4)
Cohen Syndrome (4)
Congenital Lactase Deficiency@ (1)
Congenital Pain Insensitivity@ (0)
Cornea Plana Congenita@ (2)
Cornelia De Lange Syndrome@ (2)
Costello Syndrome (2)
Cowden Syndrome (2)
Craniofrontonasal Dysplasia (3)
Cri du Chat Syndrome@ (3)
Crigler-Najjar Syndrome (6)
Currarino Syndrome (3)
Cystic Fibrosis (92)
Cystinosis@ (6)
DiGeorge Syndrome (4)
Down Syndrome (90)
Dubowitz Syndrome (3)
Dwarfism@ (25)
Ectodermal Dysplasia (5)
Ehlers-Danlos Syndrome@ (24)
Ellis-van Creveld Syndrome@ (4)
Epidermolysis Bullosa (13)
Factor V Leiden@ (4)
Familial Dysautonomia@ (7)
Familial Erythromelalgia@ (3)
Familial Hypercholesterolemia (1)
Familial Mediterranean Fever@ (8)
Fanconi Anemia@ (14)
Fatty Oxidation (4)
Floating-Harbor Syndrome (4)
Fragile X Syndrome (10)
Freeman-Sheldon Syndrome@ (5)
Friedreich Ataxia@ (12)
Fuchs' Dystrophy@ (4)
Galactosemia@ (4)
Gaucher's@ (7)
Gilbert's Syndrome (7)
Glutaricaciduria (2)
Glycogen Storage Disease Type II@ (4)
GRACILE Syndrome@ (3)
Hailey-Hailey Disease (3)
Hallervorden-Spatz Syndrome@ (2)
Hemihypertrophy (2)
Hemochromatosis (21)
Hemophilia@ (19)
Hereditary Angioedema (6)
Hereditary Spastic Paraplegia (6)
Homocystinuria@ (2)
Huntington's@ (26)
Hydrocephalus@ (35)
Hydrolethalus Syndrome (4)
Imerslund-Grasbeck Syndrome@ (2)
Incontinentia Pigmenti (5)
Jacobsen Syndrome@ (0)
Joubert Syndrome (6)
Klinefelter Syndrome (8)
Klippel-Feil Syndrome@ (6)

Langer-Giedion Syndrome@ (1)
Larsen Syndrome@ (3)
Laurence-Moon Syndrome (3)
Leber's Congenital Amaurosis@ (9)
Leigh's@ (3)
Lesch-Nyhan Syndrome (1)
Leukodystrophy@ (21)
Lissencephaly@ (3)
Loeys-Dietz Syndrome (4)
Lowe Syndrome (2)
Lymphedema@ (22)
Lysinuric Protein Intolerance@ (5)
Machado-Joseph (2)
Mannosidosis (2)
Maple Syrup Urine Disease@ (10)
Marfan Syndrome@ (20)
McArdle's (0)
MEB Disease (3)
Meckel-Gruber Syndrome (2)
Menkes' Syndrome@ (5)
Mobius Syndrome (2)
Mucolipidosis Type IV@ (4)
Mulibrey Nanism (2)
Multiple Hereditary Exostoses@ (6)
Muscular Dystrophies@ (52)
Myotonic Dystrophy@ (4)
Nail Patella Syndrome (3)
Narcolepsy@ (16)
Nasu-Hakola Disease (3)
Neurofibromatosis@ (13)
Niemann-Pick@ (4)
Noonan Syndrome (7)
Opitz Syndrome (4)
Oral-facial-digital Syndrome@ (5)
Osteogenesis Imperfecta@ (12)
Pallister Killian Mosaic Syndrome (8)
Pallister-Hall Syndrome (3)
PEHO Syndrome@ (5)
Phenylketonuria@ (8)
Polycystic Kidney@ (10)
Popliteal Pterygium Syndrome (1)
Porphyrias@ (14)
Prader-Willi Syndrome (6)
Progeria@ (9)
Propionic Acidemia (5)
Proteus Syndrome (4)
Prune Belly Syndrome (2)
Pseudoxanthoma Elasticum (5)
RAPADILINO Syndrome (2)
Refsum's@ (2)
Retinoblastoma@ (20)
Retinoschisis@ (5)
Rett's Syndrome@ (15)
Robinow Syndrome (4)
Rubinstein-Taybi Syndrome@ (6)
Russell Silver Syndrome (3)
Sanfilippo Syndrome (6)
Schizencephaly (1)
Shwachman Syndrome (7)
Sickle Cell@ (13)
Sirenomelia (6)
Smith Lemli Opitz Syndrome (3)
Smith-Magenis Syndrome (3)
Soto's Syndrome (2)
Spinal Muscular Atrophy@ (13)
Stickler's Syndrome@ (13)
Sturge-Weber Syndrome (3)
Tay-Sachs@ (4)
Thalassemia@ (20)
Thrombocytopenia Absent Radius Syndrome (2)
Tourette Syndrome@ (47)
Treacher Collins Syndrome@ (6)
Trichothiodystrophy (10)
Tuberous Sclerosis@ (11)
Turner Syndrome (12)
Tyrosinemia@ (1)
Unverricht-Lundborg Disease@ (3)
Urea Cycle (2)
Usher Syndrome (10)
VATER Syndrome@ (15)
Velo-Cardio-Facial Syndrome (5)
Von Hippel-Lindau (4)
Waardenburg Syndrome (2)
WAGR Syndrome@ (3)
Weaver Syndrome (2)
Williams Syndrome (18)
Wilson's Disease@ (9)
Wolf-Hirschhorn Syndrome (7)
Xeroderma Pigmentosum (6)
Zellweger Syndrome (4)

Gene Therapy@ (65)
Genetic Testing and Counseling@ (36)
Genetics Education@ (20)
Human Genetics@ (254)

See also:

This category in other languages:

Danish (9) Dutch (23) French (59)
German (84) Italian (43) Japanese (28)
Polish (14) Spanish (45) Swedish (1)
Turkish (4)

» http://www.geneclinics.org 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.

» http://freespace.virgin.net/andy.bowles/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.

» http://www.jewishgeneticscenter.org/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.

» http://www.kumc.edu/gec/support/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.

» http://www.ctds.info/genetic_disorders.html 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.

» http://www.immd.de/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.

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

» http://www.jdawiseman.com/papers/el-greco/el-greco-dysmorphology.html What malformation did El Greco paint? - El Greco’s faces are modelled on a child with a distinctive malformation. But what condition is it?

» http://www.xlhnetwork.org 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.

» http://www.ygyh.org Your Genes, Your Health - The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.

» http://www.newscientist.com/article/dn7445 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)

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