Halperin-Birk syndrome

Summary
Synonym
  • HLBKS
  • NEDSOSB
  • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Definition
A syndrome characterized by structural brain defects, spastic quadriplegia with multiple contractures, profound developmental delay, seizures, dysmorphism, cataract, and optic nerve atrophy that has_material_basis_in homozygous mutation in the SEC31A gene on chromosome 4q21.22.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0070539
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
22872 SEC31A SEC31 homolog A, COPII coat complex component
Displaying all 2 entries
Gene ID Gene Symbol Description Source
69162 Sec31a SEC31 homolog A, COPII coat complex component
240667 Sec31b SEC31 homolog B, COPII coat complex component
Displaying 1 entry
Gene ID Gene Symbol Description Source
851332 SEC31 Sec31p

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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