Intellectual developmental disorder with language impairment and early-onset dopa-responsive dystonia-parkinsonism

Preferred Label : Intellectual developmental disorder with language impairment and early-onset dopa-responsive dystonia-parkinsonism;

Symbol : IDLDP;

Type : Phenotype, molecular basis known;

Prefixed ID : #619911;

Details

Origin ID

619911;

UMLS CUI

C5677001;

Genes related to phenotype
- Nuclear receptor subfamily 4, group a, member 2 [OMIM gene]
ORDO concept(s)
- Autosomal dominant dopa-responsive dystonia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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