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Attention, chocolate lovers: You may not be able to help yourselves. Swiss and British scientists have linked the widespread love of chocolate to a chemical "signature" that may be programmed into our metabolic systems.
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Genetic Disorders
Aarskog Syndrome | Aase Syndrome | Ablepharon-Macrostomia Syndrome | Adrenal Hyperplasia | Alagille Syndrome | Alkaptonuria | Alopecia Areata | Alpha-1 Antitrypsin Deficiency | Angelman Syndrome | Batten | Beckwith-Wiedemann Syndrome | Canavan | Cardiac | Cardiovascular | Celiac | Cockayne Syndrome | Coffin Lowry Syndrome | Costello Syndrome | Cowden Syndrome | Craniofrontonasal Dysplasia | Crigler-Najjar Syndrome | Cystic Fibrosis | DiGeorge Syndrome | Down Syndrome | Dubowitz Syndrome | Ectodermal Dysplasia | Epidermolysis Bullosa | Familial Erythromelalgia | Familial Hypercholesterolemia | Fatty Oxidation | Floating-Harbor Syndrome | Fragile X Syndrome | Genetic Testing and Counseling | Genetics Education | Glutaricaciduria | Hailey-Hailey Disease | Hemihypertrophy | Hemochromatosis | Hereditary Angioedema | Hereditary Spastic Paraplegia | Incontinentia Pigmenti | Joubert Syndrome | Klinefelter Syndrome | Klippel-Feil Syndrome | Laurence-Moon Syndrome | Leigh's | Lesch-Nyhan Syndrome | Lowe Syndrome | Machado-Joseph | Mannosidosis | McArdle's | Meckel-Gruber Syndrome | Metabolic | Mobius Syndrome | Multiple Hereditary Exostoses | Musculoskeletal | Nail Patella Syndrome | Neurological | Noonan Syndrome | Opitz Syndrome | Organizations | Pallister-Hall Syndrome | Pallister Killian Mosaic Syndrome | Personal Pages | Popliteal Pterygium Syndrome | Prader-Willi Syndrome | Propionic Acidemia | Proteus Syndrome | Prune Belly Syndrome | Pseudoxanthoma Elasticum | Retinoblastoma | Rett's Syndrome | Robinow Syndrome | Russell Silver Syndrome | Sanfilippo Syndrome | Schizencephaly | Shwachman Syndrome | Sirenomelia | Smith-Magenis Syndrome | Smith Lemli Opitz Syndrome | Soto's Syndrome | Stickler's Syndrome | Sturge-Weber Syndrome | Support Groups | Thrombocytopenia Absent Radius Syndrome | Treacher Collins Syndrome | Trichothiodystrophy | Turner Syndrome | Urea Cycle | Urological | Usher Syndrome | Velo-Cardio-Facial Syndrome | Von Hippel-Lindau | Waardenburg Syndrome | WAGR Syndrome | Weaver Syndrome | Williams Syndrome | Xeroderma Pigmentosum | Zellweger Syndrome
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- 45, X Gonadal Dysgenesis - Turner Syndrome
- Achromatopsia - Color Blindness
- Acute Life-Threatening Episode - Apparent Life-Threatening Event
- ALTE - Apparent Life-Threatening Event
- Anembryonic Pregnancy - Blighted Ovum
- Apnea Spell - Apparent Life-Threatening Event
- Apparent Life-Threatening Event
- Autism
- Autistic Disorder - Autism
- Basal Ganglia Disorders
- Beta-Glucosidase Deficiency - Gaucher Disease
- Blighted Ovum
- CHF - Congestive Heart Failure
- Cleft Lip - Cleft Lip and Palate
- Cleft Palate - Cleft Lip and Palate
- Cleft Lip and Palate
- Color Vision Deficiency - Color Blindness
- Color Blindness
- Congenital Pernicious Anemia - Congenital Lack of Intrinsic Factor
- Congenital Lack of Intrinsic Factor
- Congestive Heart Failure
- Craniosynostosis
- Cystine Stone Disease - Cystinuria
- Cystinuria
- Developmentally Delayed - Mental Retardation
- Disorders Affecting the Basal Ganglia - Basal Ganglia Disorders
- Duchenne Muscular Dystrophy
- Dyschromatopsia - Color Blindness
- Gaucher Disease
- Genetic Counseling
- Genetic Screening
- Genetic Testing
- Gilles De La Tourette Syndrome - Tourette Syndrome
- GM2-Gangliosidosis, Type I - Tay-Sachs Disease
- Heart Failure - Congestive Heart Failure
- Hepatolenticular Degeneration - Wilson's Disease
- Hexosaminidase A Deficiency - Tay-Sachs Disease
- Huntington Chorea - Huntington Disease
- Huntington Disease
- Hyperandrogenic Chronic Anovulation - Polycystic Ovarian Syndrome
- Hyperbilirubinemia - Newborn Jaundice
- Infant Apnea - Apparent Life-Threatening Event
- Infantile Gaucher Disaese - Gaucher Disease
- Iron Level (Fe) - Serum Iron
- Juvenile Gaucher Disease - Gaucher Disease
- Klinefelter Syndrome
- Left-Sided Heart Failure - Congestive Heart Failure
- LH
- Luteinizing Hormone - LH
- Mentally Disabled - Mental Retardation
- Mental Retardation
- Monosomy X - Turner Syndrome
- Multiple Tic Syndrome - Tourette Syndrome
- Multiple Sclerosis
- Newborn Jaundice
- Oral Cleft - Cleft Lip and Palate
- Polycystic Ovarian Disorder - Polycystic Ovarian Syndrome
- Polycystic Ovarian Syndrome
- Porphyria
- Preclinical Abortion - Blighted Ovum
- Pulmonary Atresia
- Pulmonic Atresia - Pulmonary Atresia
- Serum Iron
- Stein-Leventhal Syndrome - Polycystic Ovarian Syndrome
- Tay-Sachs Disease
Related Links
- Dr. Greene's HouseCalls
- The UDGD Spot
- Primary Ciliary Dyskinesia
- Gene Clinics
- Genetic and Rare Conditions
- XLH Network
- Genetic Disorders: The Links to Diet
- Washington University in St Louis
- Your Genes, Your Health
- Blepharophimosis Ptosis Epicanthus Inversus Syndrome
- IMMD Institute of Medical Molecular Diagnostics Ltd.
- The Center For Jewish Genetics Disorders
- A3243G
- New Scientist: Heroin Addiction Gene Identified and Blocked