severe congenital neutropenia 4

Summary
Synonym
  • Dursun syndrome
  • SCN4
  • autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
  • severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome
Definition
A severe congenital neutropenia that has_material_basis_in homozygous or compound heterozygous mutation in the G6PC3 gene on chromosome 17q21.31.
Super Class
autosomal recessive disease severe congenital neutropenia
Disease Ontology
DOID:0112136
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
92579 G6PC3 glucose-6-phosphatase catalytic subunit 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
68401 G6pc3 glucose 6 phosphatase, catalytic, 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
303565 G6pc3 glucose 6 phosphatase catalytic subunit 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
790919 g6pc3 glucose-6-phosphatase catalytic subunit 3
The Human Phenotype Ontology
Displaying entries 1 - 10 of 50 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000010 Recurrent urinary tract infections
HP:0000023 Inguinal hernia
HP:0000028 Cryptorchidism
HP:0000126 Hydronephrosis
HP:0000155 Oral ulcer
HP:0000175 Cleft palate
HP:0000218 High palate
HP:0000252 Microcephaly
HP:0000365 Hearing impairment
Displaying 1 entry
Gene ID Gene Symbol Description
92579 G6PC3 glucose-6-phosphatase catalytic subunit 3

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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