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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
A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
AR AR- ARA ARB ARC ARE ARF ARG ARH ARI ARM ARN ARO ARQ ARR ARS ART ARY ARZ

arylsulfatase A deficiency

[autosomal recessive lysosomal storage disease caused by a deficiency of cerebroside sulfatase leading to an accumulation of cerebroside sulfate in the nervous system and other organs. ( CSP )]
UMLS (CSP) C0023522
 
Disease or Syndrome
Relation/PAR: LEUKODYSTROPHY
Sphingolipidoses
inborn lysosomal enzyme disorder
enzyme deficiency
Hereditary Central Nervous System Demyelinating Diseases
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