Neurodevelopmental disorder with epilepsy and brain atrophy

Preferred Label : Neurodevelopmental disorder with epilepsy and brain atrophy;

Symbol : NEDEBA;

Type : Phenotype, molecular basis known;

Prefixed ID : #619971;

Details

Origin ID

619971;

UMLS CUI

C5774184;

Genes related to phenotype
- Atpase, h+ transporting, lysosomal, v0 subunit a1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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