Developmental delay, language impairment, and ocular abnormalities

Preferred Label : Developmental delay, language impairment, and ocular abnormalities;

Symbol : DEVLO;

Type : Phenotype, molecular basis known;

Prefixed ID : #620141;

Details

Origin ID

620141;

UMLS CUI

C5774262;

Genes related to phenotype
- Actin-related protein 2/3 complex, subunit 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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