UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
U U- U0 U5 U7 UA UB UC UD UE UG UK UL UM UN UP UR US UT UU UV UZ
USA USC USD USE USH USM USN USU

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

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