Bryant-LI-bhoj neurodevelopmental syndrome 2

Preferred Label : Bryant-LI-bhoj neurodevelopmental syndrome 2;

Symbol : BRYLIB2;

Type : Phenotype, molecular basis known;

Prefixed ID : #619721;

Details

Origin ID

619721;

UMLS CUI

C5676906;

Genes related to phenotype
- H3 histone, family 3b [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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