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Genetic Disorders


Directory > Health > Conditions_and_Diseases > Genetic Disorders

Aarskog_Syndrome (4)Aase_Syndrome (3)Ablepharon-Macrostomia_Syndrome (4)
Acoustic_Neuroma@ (15)Adie_Syndrome@ (3)Adrenal_Hyperplasia@ (6)
Adrenoleukodystrophy@ (6)Aicardi_Syndrome@ (7)Alagille_Syndrome (8)
Albinism@ (12)Alfi's_Syndrome (2)Alkaptonuria (4)
Alopecia_Areata@ (13)Alpha-1_Antitrypsin_Deficiency (11)Alstrom_Syndrome@ (3)
Angelman_Syndrome@ (21)Apert_Syndrome@ (10)Arthrogryposis@ (65)
Aspartylglucosaminuria@ (3)Ataxia@ (8)Autism@ (544)
Bardet-Biedl_Syndrome@ (3)Barth_Syndrome@ (3)Batten_Disease (8)
Beckwith-Wiedemann_Syndrome (7)Bloom_Syndrome (5)Branchio-Oto-Renal_Syndrome (6)
Canavan@ (4)Cardiac@ (50)Cardiovascular@ (5)
Celiac@ (55)Cerebrocostomandibular_Syndrome@ (2)Charcot-Marie-Tooth_Disease@ (7)
Choroideremia@ (4)Cleidocranial_Dysplasia@ (3)Cockayne_Syndrome@ (3)
Coffin_Lowry_Syndrome (4)Cohen_Syndrome (4)Congenital_Lactase_Deficiency@ (2)
Cornea_Plana_Congenita@ (2)Cornelia_De_Lange_Syndrome@ (4)Costello_Syndrome (2)
Cowden_Syndrome (3)Craniofrontonasal_Dysplasia (3)Cri_du_Chat_Syndrome@ (4)
Crigler-Najjar_Syndrome (7)Currarino_Syndrome (4)Cystic_Fibrosis (129)
Cystinosis@ (8)DiGeorge_Syndrome (4)Down_Syndrome (103)
Dubowitz_Syndrome (3)Dwarfism@ (29)Ectodermal_Dysplasia (6)
Ehlers-Danlos_Syndrome@ (28)Ellis-van_Creveld_Syndrome@ (5)Epidermolysis_Bullosa (17)
Factor_V_Leiden@ (4)Familial_Dysautonomia@ (8)Familial_Erythromelalgia@ (3)
Familial_Hypercholesterolemia (1)Familial_Mediterranean_Fever@ (8)Fanconi_Anemia@ (12)
Fatty_Oxidation (5)Floating-Harbor_Syndrome (4)Fragile_X_Syndrome (12)
Freeman-Sheldon_Syndrome@ (5)Friedreich_Ataxia@ (12)Fuchs'_Dystrophy@ (4)
Galactosemia@ (6)Gaucher's@ (13)Gene_Therapy@ (69)
Genetic_Testing_and_Counseling@ (24)Genetics_Education@ (17)Gilbert's_Syndrome (10)
Glutaricaciduria (3)Glycogen_Storage_Disease_Type_II@ (5)GRACILE_Syndrome@ (3)
Hailey-Hailey_Disease (4)Hallervorden-Spatz_Syndrome@ (3)Hemihypertrophy (3)
Hemochromatosis (25)Hemophilia@ (27)Hereditary_Angioedema (6)
Hereditary_Spastic_Paraplegia (7)Homocystinuria@ (2)Human_Genetics@ (229)
Huntington's@ (27)Hydrocephalus@ (42)Hydrolethalus_Syndrome (4)
Imerslund-Grasbeck_Syndrome@ (2)Incontinentia_Pigmenti (7)Joubert_Syndrome (7)
Klinefelter_Syndrome (9)Klippel-Feil_Syndrome@ (7)Langer-Giedion_Syndrome@ (2)
Larsen_Syndrome@ (4)Laurence-Moon_Syndrome (3)Leber's_Congenital_Amaurosis@ (10)
Leigh's@ (4)Lesch-Nyhan_Syndrome (1)Leukodystrophy@ (26)
Lissencephaly@ (6)Loeys-Dietz_Syndrome (5)Lowe_Syndrome (2)
Lymphedema@ (25)Lysinuric_Protein_Intolerance@ (5)Machado-Joseph (3)
Mannosidosis (2)Maple_Syrup_Urine_Disease@ (10)Marfan_Syndrome@ (25)
McArdle's (1)MEB_Disease (3)Meckel-Gruber_Syndrome (2)
Menkes'_Syndrome@ (6)Metabolic@ (378)Mobius_Syndrome (5)
Mucolipidosis_Type_IV@ (4)Mulibrey_Nanism (2)Multiple_Hereditary_Exostoses@ (6)
Muscular_Dystrophies@ (65)Musculoskeletal@ (203)Myotonic_Dystrophy@ (4)
Nail_Patella_Syndrome (5)Narcolepsy@ (20)Nasu-Hakola_Disease (3)
Neurofibromatosis@ (17)Neurological@ (109)Niemann-Pick@ (4)
Noonan_Syndrome (8)Opitz_Syndrome (5)Organizations (8)
Osteogenesis_Imperfecta@ (14)Pallister-Hall_Syndrome (3)Pallister_Killian_Mosaic_Syndrome (9)
PEHO_Syndrome@ (5)Personal_Pages (12)Phenylketonuria@ (9)
Polycystic_Kidney@ (14)Popliteal_Pterygium_Syndrome (1)Porphyrias@ (14)
Prader-Willi_Syndrome (9)Progeria@ (10)Propionic_Acidemia (5)
Proteus_Syndrome (5)Prune_Belly_Syndrome (2)Pseudoxanthoma_Elasticum (5)
RAPADILINO_Syndrome (3)Refsum's@ (3)Retinoblastoma@ (24)
Retinoschisis@ (7)Rett's_Syndrome@ (19)Robinow_Syndrome (4)
Rubinstein-Taybi_Syndrome@ (4)Russell_Silver_Syndrome (3)Sanfilippo_Syndrome (7)
Schizencephaly (1)Shwachman_Syndrome (7)Sickle_Cell@ (19)
Sirenomelia (6)Smith-Magenis_Syndrome (3)Smith_Lemli_Opitz_Syndrome (3)
Soto's_Syndrome (5)Spinal_Muscular_Atrophy@ (16)Stickler's_Syndrome@ (4)
Sturge-Weber_Syndrome (4)Support_Groups@ (26)Tay-Sachs@ (4)
Thalassemia@ (21)Thrombocytopenia_Absent_Radius_Syndrome (3)Tourette_Syndrome@ (57)
Treacher_Collins_Syndrome@ (4)Trichothiodystrophy (10)Tuberous_Sclerosis@ (12)
Turner_Syndrome (13)Tyrosinemia@ (2)Unverricht-Lundborg_Disease@ (3)
Urea_Cycle (2)Urological@ (25)Usher_Syndrome (2)
VATER_Syndrome@ (18)Velo-Cardio-Facial_Syndrome (5)Von_Hippel-Lindau (4)
Waardenburg_Syndrome (2)WAGR_Syndrome@ (3)Weaver_Syndrome (2)
Williams_Syndrome (17)Wilson's_Disease@ (11)Wolf-Hirschhorn_Syndrome (8)
Xeroderma_Pigmentosum (6)Zellweger_Syndrome (7)
 
Related Categories:
   Health > Conditions_and_Diseases > Rare_Disorders (122)
   Health > Conditions_and_Diseases > Congenital_Anomalies (3)


56 Listings - DR (8/10)56 Listings - DR (8/10) New Scientist: Heroin Addiction Gene Identified and Blocked - http://www.newscientist.com/article.ns?id=dn7445
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.
1,441 Listings - DR (6/10)1,441 Listings - DR (6/10) Blepharophimosis Ptosis Epicanthus Inversus Syndrome - http://freespace.virgin.net/andy.bowles/
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.
On Target - DR (5/10)On Target - DR (5/10) IMMD Institute of Medical Molecular Diagnostics Ltd. - http://www.immd.de/
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.
5 Listings - DR (5/10)5 Listings - DR (5/10) Your Genes, Your Health - http://www.ygyh.org
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
15 Listings - DR (4/10)15 Listings - DR (4/10) Genetic Disorders: The Links to Diet - http://www.ctds.info/genetic_disorders.html
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.
8 Listings - DR (4/10)8 Listings - DR (4/10) Information on Trisomy 13 - http://www.drgreene.org/body.cfm?id=21&action=detail&ref=614
Discusses medical information on this chromosome abnormality, including the doctor's personal experience with this rare disease.
On Target - DR (4/10)On Target - DR (4/10) Primary Ciliary Dyskinesia - http://www.p-c-d.org/en/
Information on a rare congenital disease.
11 Listings - DR (4/10)11 Listings - DR (4/10) Gene Clinics - http://www.geneclinics.org
Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
71 Listings - DR (4/10)71 Listings - DR (4/10) Genetic and Rare Conditions - http://www.kumc.edu/gec/support/
Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
On Target - DR (3/10)On Target - DR (3/10) The Center For Jewish Genetics Disorders - http://www.jewishgeneticscenter.org/
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.
16 Listings - DR (3/10)16 Listings - DR (3/10) What malformation did El Greco paint? - http://www.jdawiseman.com/papers/el-greco/el-greco-dysmorphology.html
El Greco’s faces are modelled on a child with a distinctive malformation. But what condition is it?
On Target - DR (2/10)On Target - DR (2/10) A3243G - http://www.a3243g.com/
Explains a gene defect of mitochondrial DNA which causes several diseases, including maternally inherited diabetes with deafness. Features a newsletter, patient forum and definitions.
On Target - DR (2/10)On Target - DR (2/10) XLH Network - http://www.xlhnetwork.org
Patient support group for XLH, a genetic condition also known as X-Linked Hypophosphatemia, X-Linked Hypophosphatemic Rickets, Familial Hypophosphatemia, Vitamin D-Resistant Rickets.

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