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Albinism deafness syndrome
Also Known As:
Albinism-Deafness Syndrome
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Eye Diseases: 3522
Hereditary Eye Diseases: 18
Albinism: 486
Albinism deafness syndrome: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Inborn Errors Amino Acid Metabolism: 1
Albinism: 486
Albinism deafness syndrome: 1
Genetic Skin Diseases: 47
Albinism: 486
Albinism deafness syndrome: 1
Hereditary Eye Diseases: 18
Albinism: 486
Albinism deafness syndrome: 1
Skin and Connective Tissue Diseases
Skin Diseases: 13127
Pigmentation Disorders: 149
Hypopigmentation: 836
Albinism: 486
Albinism deafness syndrome: 1
Genetic Skin Diseases: 47
Albinism: 486
Albinism deafness syndrome: 1
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Inborn Errors Amino Acid Metabolism: 1
Albinism: 486
Albinism deafness syndrome: 1
Otorhinolaryngologic Diseases: 203
Ear Diseases: 261
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Albinism deafness syndrome: 1
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Albinism deafness syndrome: 1
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Albinism deafness syndrome: 1
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Albinism deafness syndrome:
1.
Complementary DNA (cDNA)
IBA
03/01/1998 - "
We have employed a direct cDNA selection methodology to isolate transcribed sequences encoded in the human chromosomal interval Xq26 that contains the gene for X-chromosome linked albinism deafness syndrome (ADFN).
"