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Robinson Miller Bensimon syndrome
Familial ectodermal dysplasia with sensori-neural deafness and other anomalies
Also Known As:
Deafness and onychodystrophy, dominant form
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Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
Multiple Abnormalities: 211
Ectodermal Dysplasia: 505
Robinson Miller Bensimon syndrome
Skin Abnormalities: 159
Ectodermal Dysplasia: 505
Robinson Miller Bensimon syndrome
Inborn Genetic Diseases: 11939
Genetic Skin Diseases: 47
Ectodermal Dysplasia: 505
Robinson Miller Bensimon syndrome
Skin and Connective Tissue Diseases
Skin Diseases: 13127
Skin Abnormalities: 159
Ectodermal Dysplasia: 505
Robinson Miller Bensimon syndrome
Genetic Skin Diseases: 47
Ectodermal Dysplasia: 505
Robinson Miller Bensimon syndrome
Otorhinolaryngologic Diseases: 203
Ear Diseases: 261
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Robinson Miller Bensimon syndrome
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Robinson Miller Bensimon syndrome
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Robinson Miller Bensimon syndrome