Greenberg dysplasia

Summary
Synonym
  • GRBGD
  • Greenberg skeletal dysplasia
  • HEM dysplasia
  • Skeletal dysplasia, Greenberg type
  • autosomal recessive lethal chondrodystrophy with congenital hydrops
  • hydrops, ectopic calcification, moth-eaten skeletal dysplasia
  • hydrops-ectopic calcification-motheaten syndrome
Definition
An inherited metabolic disorder characterized by a defect in cholesterol biosynthesis resulting in fetal hydrops, severe shortening of all long bones with a moth-eaten radiographic appearance, platyspondyly, disorganization of chondroosseous calcification, and ectopic ossification centers that has_material_basis_in homozygous or compound heterozygous mutation in LBR on chromosome 1q42.12.
Super Class
autosomal recessive disease inherited metabolic disorder
Disease Ontology
DOID:0111588
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3930 LBR lamin B receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source
98386 Lbr lamin B receptor

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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