heterotopia, periventricular nodular, with frontometaphyseal dysplasia

Preferred Label : heterotopia, periventricular nodular, with frontometaphyseal dysplasia;

Origin ID

C564725;

UMLS CUI

C1848214;

Automatic exact mappings (from CISMeF team)
- Periventricular nodular heterotopia 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- osteochondrodysplasias [MeSH Descriptor]
- periventricular nodular heterotopia [MeSH Descriptor]
Record concept(s)
- heterotopia, periventricular nodular, with frontometaphyseal dysplasia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]