ManofKnowledge.com | Aarskog Syndrome | Aase Syndrome | Ablepharon-Macrostomia Syndrome | Alagille Syndrome

Aarskog Syndrome | Aase Syndrome | Ablepharon-Macrostomia Syndrome | Alagille Syndrome | Genetic Disorders Alkaptonuria
Aarskog Syndrome | Aase Syndrome | Ablepharon-Macrostomia Syndrome | Alagille Syndrome | Genetic Disorders Alkaptonuria

Search the following categories:,Beckwith-Wiedemann Syndrome,Cystic Fibrosis,Down Syndrome,Epidermolysis Bullosa,Aarskog Syndrome,Aase Syndrome,Ablepharon-Macrostomia Syndrome,Alagille Syndrome,Alkaptonuria,Alpha-1 Antitrypsin Deficiency,Batten,Coffin Lowry Syndrome,Costello Syndrome,Cowden Syndrome,Craniofrontonasal Dysplasia,Crigler-Najjar Syndrome,DiGeorge Syndrome,Dubowitz Syndrome,Ectodermal Dysplasia,Familial Hypercholesterolemia,Fatty Oxidation,Floating-Harbor Syndrome,Fragile X Syndrome,Glutaricaciduria,Hailey-Hailey Disease,Hemihypertrophy,Hemochromatosis,Hereditary Angioedema,Hereditary Spastic Paraplegia,Incontinentia Pigmenti,Joubert Syndrome,Klinefelter Syndrome,Laurence-Moon Syndrome,Lesch-Nyhan Syndrome,Lowe Syndrome,Machado-Joseph,Mannosidosis,McArdle's,Meckel-Gruber Syndrome,Mobius Syndrome,Nail Patella Syndrome,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,Robinow Syndrome,Russell Silver Syndrome,Sanfilippo Syndrome,Schizencephaly,Shwachman Syndrome,Sirenomelia,Smith-Magenis Syndrome,Smith Lemli Opitz Syndrome,Soto's Syndrome,Sturge-Weber Syndrome,Thrombocytopenia Absent Radius Syndrome,Trichothiodystrophy,Turner Syndrome,Urea Cycle,Usher Syndrome,Velo-Cardio-Facial Syndrome,Von Hippel-Lindau,Waardenburg Syndrome,Weaver Syndrome,Williams Syndrome,Xeroderma Pigmentosum,Zellweger Syndrome,

Top/Health/Conditions and Diseases/Genetic Disorders

Beckwith-Wiedemann Syndrome

Cystic Fibrosis

Down Syndrome

Epidermolysis Bullosa

Aarskog Syndrome

Aase Syndrome

Ablepharon-Macrostomia Syndrome

Alagille Syndrome

Alkaptonuria

Alpha-1 Antitrypsin Deficiency

Batten

Coffin Lowry Syndrome

Costello Syndrome

Cowden Syndrome

Craniofrontonasal Dysplasia

Crigler-Najjar Syndrome

DiGeorge Syndrome

Dubowitz Syndrome

Ectodermal Dysplasia

Familial Hypercholesterolemia

Fatty Oxidation

Floating-Harbor Syndrome

Fragile X Syndrome

Glutaricaciduria

Hailey-Hailey Disease

Hemihypertrophy

Hemochromatosis

Hereditary Angioedema

Hereditary Spastic Paraplegia

Incontinentia Pigmenti

Joubert Syndrome

Klinefelter Syndrome

Laurence-Moon Syndrome

Meckel-Gruber Syndrome

Mobius Syndrome

Nail Patella Syndrome

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

Robinow Syndrome

Russell Silver Syndrome

Smith-Magenis Syndrome

Smith Lemli Opitz Syndrome

Soto's Syndrome

Sturge-Weber Syndrome

Thrombocytopenia Absent Radius Syndrome

Velo-Cardio-Facial Syndrome

Xeroderma Pigmentosum

Zellweger Syndrome

A3243G
Explains a gene defect which causes several diseases including Maternally Inherited Diabetes with Deafness. Features a newsletter, forum and definitions.

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.

Dr. Greene's HouseCalls
A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.

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.

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.

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.

Primary Ciliary Dyskinesia
Information on a rare congenital disease.

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.

The UDGD Spot
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.

Washington University in St Louis
Family resource for individuals with Papillon Lefevre, Haim-Munk Syndrome and Prepubertal Periodontis. Interested families may participate in a registry dedicated to learning about the natural history of these three conditions.

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.

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