Neurodegeneration, childhood-onset, with progressive microcephaly

Preferred Label : Neurodegeneration, childhood-onset, with progressive microcephaly;

Symbol : CONPM;

Type : Phenotype, molecular basis known;

Prefixed ID : #619847;

Details

Origin ID

619847;

UMLS CUI

C5676972;

Genes related to phenotype
- Deoxythymidylate kinase [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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