Gaucher's disease perinatal lethal

Summary
Synonym
  • Fetal Gaucher Disease
  • Gaucher Disease, Collodion Type
Definition
A Gaucher's Disease characterized by perinatal lethality and rapid progression of neurological deterioration that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22.
Super Class
Gaucher's disease
External Links
Disease Ontology
DOID:0110960
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2629 GBA1 glucosylceramidase beta 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14466 Gba1 glucosylceramidase beta 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
177314 gba-4 Putative glucosylceramidase 4
178535 gba-3 Putative glucosylceramidase 3
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P04062 Lysosomal acid glucosylceramidase
The Human Phenotype Ontology
Displaying entries 31 - 40 of 64 in total
HPO ID HPO Term
HP:0000316 Hypertelorism
HP:0000325 Triangular face
HP:0000347 Micrognathia
HP:0000369 Low-set ears
HP:0000486 Strabismus
HP:0000741 Apathy
HP:0000962 Hyperkeratosis
HP:0000967 Petechiae
HP:0000979 Purpura
HP:0001399 Hepatic failure
Displaying 1 entry
Gene ID Gene Symbol Description
2629 GBA1 glucosylceramidase beta 1

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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: August 19, 2024