Leukodystrophy, childhood-onset, remitting

Preferred Label : Leukodystrophy, childhood-onset, remitting;

Symbol : CORLK;

Type : Phenotype, molecular basis known;

Prefixed ID : #619864;

Détails

Origin ID

619864;

UMLS CUI

C5676979;

Genes related to phenotype
- Fructose-1,6-bisphosphatase 2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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