Neurodevelopmental disorder with central hypotonia and dysmorphic facies

Preferred Label : Neurodevelopmental disorder with central hypotonia and dysmorphic facies;

Symbol : NEDCHF;

Type : Phenotype, molecular basis known;

Prefixed ID : #619797;

Détails

Origin ID

619797;

UMLS CUI

C5676944;

Genes related to phenotype
- Histone deacetylase 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients