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Ermine phenotype
Also Known As:
Cutaneous albinism hermine phenotype; O'Doherty syndrome; Pigmentary disorder with hearing loss
Networked:
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Disease Context: Research Results
Otorhinolaryngologic Diseases: 203
Ear Diseases: 261
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Ermine phenotype
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Ermine phenotype
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Ermine phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Inborn Errors Amino Acid Metabolism: 1
Albinism: 486
Piebaldism: 75
Ermine phenotype
Genetic Skin Diseases: 47
Albinism: 486
Piebaldism: 75
Ermine phenotype
Hereditary Eye Diseases: 18
Albinism: 486
Piebaldism: 75
Ermine phenotype
Skin and Connective Tissue Diseases
Skin Diseases: 13127
Pigmentation Disorders: 149
Hypopigmentation: 836
Albinism: 486
Piebaldism: 75
Ermine phenotype
Genetic Skin Diseases: 47
Albinism: 486
Piebaldism: 75
Ermine phenotype
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Inborn Errors Amino Acid Metabolism: 1
Albinism: 486
Piebaldism: 75
Ermine phenotype