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Genetic Disorders
Directory > Health > Conditions_and_Diseases > Genetic Disorders
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| Health > Conditions_and_Diseases > Congenital_Anomalies (3) |
| Health > Conditions_and_Diseases > Rare_Disorders (115) |
  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. |
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. |
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. |
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. |
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. |
Discusses medical information on this chromosome abnormality, including the doctor's personal experience with this rare disease. |
Information on a rare congenital disease. |
Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. |
Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. |
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. |
El Greco’s faces are modelled on a child with a distinctive malformation. But what condition is it? |
Explains a gene defect of mitochondrial DNA which causes several diseases, including maternally inherited diabetes with deafness. Features a newsletter, patient forum and definitions. |
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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