mucolipidosis III alpha/beta

Summary
Synonym
  • mucolipidosis III
  • pseudo-Hurler polydystrophy
Definition
A mucolipidosis that has_material_basis_in mutation in the gene encoding the alpha/beta-subunits precursor gene of GLcNAc-phosphotransferase.
Super Class
autosomal recessive disease mucolipidosis
External Links
Disease Ontology
DOID:0080071
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
2720 GLB1 galactosidase beta 1
10724 OGA O-GlcNAcase
51172 NAGPA N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
84572 GNPTG N-acetylglucosamine-1-phosphate transferase subunit gamma
Displaying 1 entry
Gene ID Gene Symbol Description Source
432486 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
Displaying 1 entry
Gene ID Gene Symbol Description Source
553365 gnptab N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
The Human Phenotype Ontology
Displaying entries 11 - 20 of 70 in total
HPO ID HPO Term
HP:0000405 Conductive hearing impairment
HP:0008897 Postnatal growth retardation
HP:0001537 Umbilical hernia
HP:0012185 Constrictive median neuropathy
HP:0001653 Mitral regurgitation
HP:0000943 Dysostosis multiplex
HP:0002797 Osteolysis
HP:0000212 Gingival overgrowth
HP:0002355 Difficulty walking
HP:0000403 Recurrent otitis media
Displaying 1 entry
Gene ID Gene Symbol Description
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta

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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