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
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
Sphingolipidoses
inborn lysosomal enzyme disorder
enzyme deficiency
Hereditary Central Nervous System Demyelinating Diseases
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