Usher syndrome
[hereditary disorder believed to occur in two forms: (1) characterized by congenital deafness and severe retinitis pigmentosa, and (2) in which the inner ear and retina are less severely affected; most cases are transmitted as autosomal recessive trait, but some forms are X-linked. ( CSP )]
UMLS (CSP) C0271097- Congenital Abnormality
- Disease or Syndrome
Relation/PAR: Genetic Condition
retinitis pigmentosa
congenital deafness
retinitis pigmentosa
congenital deafness
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