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Autosomal dominant deafness -onychodystrophy syndrome
Did you mean Autosomal dominant deafness -"onycho dystrophy" syndrome?
- ... disorder in their family. ADCA-DN syndrome ADCADN Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Genetic ...
- ... National Organization for Rare Disorders (NORD) KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT; KIDAD KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE; KIDAR ...
- Degenerative Nerve Diseases (National Library of Medicine)Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. ...
- ... bones, nerve tissue, and muscles seen in craniofacial-deafness-hand syndrome. PAX3 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... COL4A3 or COL4A4 gene have progressive kidney disease (autosomal dominant Alport syndrome) and others have ... syndrome Hematuric hereditary nephritis Hemorrhagic familial nephritis Hemorrhagic ...
- ... Organization for Rare Disorders (NORD) KERATODERMA, PALMOPLANTAR, WITH DEAFNESS PubMed Birkenhager R, Lublinghoff N, Prera E, Schild C, Aschendorff A, Arndt S. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W ...
- ... syndrome. SALL1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Anal-ear-renal-radial malformation syndrome Deafness-imperforate anus-hypoplastic thumbs syndrome Imperforate anus-hand ...
- ... mutations. MITF ... of Tietz Hypopigmentation-deafness syndrome Hypopigmentation/deafness of Tietz Tietz albinism-deafness syndrome ...
- ... of signs and symptoms associated with Baraitser-Winter syndrome. More About This Health Condition ... gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 DFNA26 gamma- ...
- ... and symptoms of the condition. ... dysplasia, autosomal recessive Otospondylomegaepiphyseal ...
