Neurodevelopmental disorder with speech or visual impairment and brain hypomyelination

Preferred Label : Neurodevelopmental disorder with speech or visual impairment and brain hypomyelination;

Symbol : NEDSVH;

Type : Phenotype, molecular basis known;

Prefixed ID : #621034;

Details

Origin ID

621034;

Genes related to phenotype
- Chaperonin containing t-complex polypeptide 1, subunit 3 [OMIM gene]

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