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
AD AD ADA ADB ADC ADD ADE ADF ADH ADI ADJ ADL ADM ADN ADO ADP ADR ADS ADT ADU ADV

adrenoleukodystrophy

[childhood genetic disease, transmitted as an X-linked recessive trait, characterized by diffuse abnormality of cerebral white matter and adrenal atrophy; mental deterioration progresses to dementia, aphasia, apraxia, dysarthria, and loss of vision. ( CSP )]
UMLS (CSP) C0162309
 
Disease or Syndrome
Relation/PAR: adrenal disorder
Adrenal Gland Hypofunction
Genetic Condition
LEUKODYSTROPHY
Sphingolipidoses
PEROXISOMAL DISORDERS
Hereditary Central Nervous System Demyelinating Diseases

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