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Items: 3

1.

Neurological phenotype

MedGen UID:
833938
Concept ID:
CN230745
Finding
2.

Abnormal CNS myelination

An abnormality of myelination of nerves in the central nervous system. [from HPO]

MedGen UID:
760153
Concept ID:
CN167128
Finding
3.

Childhood-onset cerebral X-linked adrenoleukodystrophy

MedGen UID:
430754
Concept ID:
CN036464
Disease or Syndrome
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