Medical References
Diseases & Conditions
Women's Health
Mental Health
Men's Health
Medical Web Links
MOL Site Map
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.
Read more health news
Medical Reference
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
(73)
- Apparent Life-Threatening Event
- Autism
- Duchenne Muscular Dystrophy
- Hyperandrogenic Chronic Anovulation - Polycystic Ovarian Syndrome
- Newborn Jaundice
- Polycystic Ovarian Syndrome
- ALTE - Apparent Life-Threatening Event
- Apnea Spell - Apparent Life-Threatening Event
- CHF - Congestive Heart Failure
- Cleft Lip - Cleft Lip and Palate
- Congenital Pernicious Anemia - Congenital Lack of Intrinsic Factor
- Gilles De La Tourette Syndrome - Tourette Syndrome
- Huntington Disease
- Luteinizing Hormone - LH
- Achromatopsia - Color Blindness
- Aneurysm, Brain
- Disorders Affecting the Basal Ganglia - Basal Ganglia Disorders
- Genetic Counseling
- Heart Failure - Congestive Heart Failure
- Pulmonary Atresia
- Pulmonic Atresia - Pulmonary Atresia
- Stein-Leventhal Syndrome - Polycystic Ovarian Syndrome
- Color Blindness
- Congenital Lack of Intrinsic Factor
- Craniosynostosis
- Cystinuria
- FSH
- Infant Apnea - Apparent Life-Threatening Event
- Infant Milestones
- Polycystic Ovarian Disorder - Polycystic Ovarian Syndrome
- Color Vision Deficiency - Color Blindness
- Developmentally Delayed - Mental Retardation
- Genetic Testing
- Infantile Gaucher Disaese - Gaucher Disease
- Osteoporosis
- Preclinical Abortion - Blighted Ovum
- Skin Cancer
- Tay-Sachs Disease
- 45, X Gonadal Dysgenesis - Turner Syndrome
- Acute Life-Threatening Episode - Apparent Life-Threatening Event
- Anembryonic Pregnancy - Blighted Ovum
- Genetic Screening
- Huntington Chorea - Huntington Disease
- Mental Retardation
- Multiple Sclerosis
- Porphyria
- Serum Iron
- Autistic Disorder - Autism
- Basal Ganglia Disorders
- Blighted Ovum
- Cleft Lip and Palate
- Cystine Stone Disease - Cystinuria
- Follicle-Stimulating Hormone - FSH
- Gaucher Disease
- Hepatolenticular Degeneration - Wilson's Disease
- Hexosaminidase A Deficiency - Tay-Sachs Disease
- Huntington Disease Dementia
- Hyperbilirubinemia - Newborn Jaundice
- LH
- Monosomy X - Turner Syndrome
- Autism
- Beta-Glucosidase Deficiency - Gaucher Disease
- Cleft Palate - Cleft Lip and Palate
- Congestive Heart Failure
- Dyschromatopsia - Color Blindness
- GM2-Gangliosidosis, Type I - Tay-Sachs Disease
- In Vitro Fertilization
- Iron Level (Fe) - Serum Iron
- Juvenile Gaucher Disease - Gaucher Disease
- Klinefelter Syndrome
- Left-Sided Heart Failure - Congestive Heart Failure
- Mentally Disabled - Mental Retardation
- Multiple Tic Syndrome - Tourette Syndrome
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