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
External Links
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 31 - 40 of 50 in total
HPO ID HPO Term
HP:0001903 Anemia
HP:0002092 Pulmonary arterial hypertension
HP:0002093 Respiratory insufficiency
HP:0002205 Recurrent respiratory infections
HP:0002240 Hepatomegaly
HP:0002619 Varicose veins
HP:0002718 Recurrent bacterial infections
HP:0002783 Recurrent lower respiratory tract infections
HP:0002788 Recurrent upper respiratory tract infections
HP:0003198 Myopathy
Displaying 1 entry
Gene ID Gene Symbol Description
92579 G6PC3 glucose-6-phosphatase catalytic subunit 3

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Last updated: August 19, 2024