proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome

Summary
Synonym
  • EPV
  • Fowler syndrome
  • Fowler vasculopathy
  • PVHH
  • cerebral proliferative glomeruloid vasculopathy
  • encephaloclastic proliferative vasculopathy
  • hydranencephaly, Fowler type
  • hydrocephaly/hydranencephaly due to cerebral vasculopathy
  • proliferative vasculopathy and hydranencephaly/hydrocephaly
Definition
A syndrome characterized by hydranencephaly, glomeruloid vasculopathy of the central nervous system and retinal vessels, diffuse clastic ischemic lesions of the brain stem, basal ganglia, and spinal cord with calcifications, and fetal akinesia with arthrogryposis that has_material_basis_in homozygous or compound heterozygous mutation in the FLVCR2 gene on chromosome 14q24.3.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0111666
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
11988 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2
11989 Slc7a3 solute carrier family 7 (cationic amino acid transporter, y+ system), member 3
Displaying all 2 entries
Gene ID Gene Symbol Description Source
29485 Slc7a3 solute carrier family 7 member 3
64554 Slc7a2 solute carrier family 7 member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
494041 slc7a2 solute carrier family 7 member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
852803 HNM1 Hnm1p

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024