encephaloclastic proliferative vasculopathy

Preferred Label : encephaloclastic proliferative vasculopathy;

MeSH note : mutation in FLVCR2;

MeSH synonym : hydranencephaly, fowler type; Hydrocephaly-Hydranencephaly due to Cerebral Vasculopathy;

Details

Origin ID

C565593;

UMLS CUI

C1856972;

Currated CISMeF NLP mapping
- Fowler vasculopathy [ORDO Disease]
- Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [OMIM Phenotype]
- proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [DO Concept]
DO Cross reference
- proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [DO Concept]
MeSH term(s) associated for indexing
- hydranencephaly [MeSH Descriptor]
Record concept(s)
- encephaloclastic proliferative vasculopathy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fowler vasculopathy [ORDO Disease]
- Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [OMIM Phenotype]

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